High density plate filler

ABSTRACT

A filling apparatus for filling a microplate. The microplate having a plurality of wells each sized to receive an assay. The filling apparatus can comprise an output layer having a plurality of capillaries, wherein a first grouping of the capillaries is separated from a second grouping by a hydrophobic feature. Each of the plurality of capillaries can comprise an inlet and an outlet. A funnel assembly can comprise a funnel member sized to receive the assay. The funnel member can comprise an outlet for delivering a fluid bead of the assay along a top surface of the output layer and in fluid communication with each of the plurality of capillaries such that a portion of the fluid bead can be drawn within at least some of the plurality of capillaries in response to capillary force. The funnel assembly and the output layer can be moveable relative to each other between a first position and a second position to draw the fluid bead across the top surface.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation-in-part of U.S. patent applicationSer. No. 11/086,800 filed on Mar. 22, 2005 now abandoned. U.S. patentapplication Ser. No. 11/086,800 is a continuation-in-part of U.S. patentapplication Ser. No. 10/944,673 filed on Sep. 17, 2004, now abandonedand U.S. patent application Ser. No. 10/944,691 filed on Sep. 17, 2004now abandoned.

U.S. patent application Ser. No. 10/944,673 claims a benefit to U.S.Provisional Application No. 60/504,500 filed on Sep. 19, 2003; U.S.Provisional Application No. 60/504,052 filed on Sep. 19, 2003; U.S.Provisional Application No. 60/589,224 filed Jul. 19, 2004; U.S.Provisional Application No. 60/589,225 filed on Jul. 19, 2004; and U.S.Provisional Application No. 60/601,716 filed on Aug. 13, 2004.

U.S. patent application Ser. No. 10/944,691 is a continuation-in-part ofU.S. patent application Ser. No. 10/913,601 filed on Aug. 5, 2004 nowU.S. Pat. No. 7,233,393 and claims the benefit of U.S. ProvisionalApplication No. 60/504,052 filed on Sep. 19, 2003; U.S. ProvisionalApplication No. 60/504,500 filed on Sep. 19, 2003; U.S. ProvisionalApplication No. 60/589,224 filed Jul. 19, 2004; U.S. ProvisionalApplication No. 60/589,225 filed on Jul. 19, 2004; and U.S. ProvisionalApplication No. 60/601,716 filed on Aug. 13, 2004.

All literature and similar materials cited in this application,including but not limited to, patents, patent applications, articles,books, treatises, and internet web pages, regardless of the format ofsuch literature and similar materials, are expressly incorporated byreference in their entirety for any purpose. In the event that one ormore of the incorporated literature and similar materials differs fromor contradicts this application, including but not limited to definedterms, term usage, described techniques, or the like, this applicationcontrols.

INTRODUCTION

Currently, genomic analysis, including that of the estimated 30,000human genes is a major focus of basic and applied biochemical andpharmaceutical research. Such analysis may aid in developingdiagnostics, medicines, and therapies for a wide variety of disorders.However, the complexity of the human genome and the interrelatedfunctions of genes often make this task difficult. There is a continuingneed for methods and apparatus to aid in such analysis.

DRAWINGS

The skilled artisan will understand that the drawings, described herein,are for illustration purposes only. The drawings are not intended tolimit the scope of the present teachings in any way.

FIG. 1 is a perspective view illustrating a high-density sequencedetection system according to some embodiments of the present teachings;

FIG. 2 is a top perspective view illustrating a microplate in accordancewith some embodiments;

FIG. 3 is a top perspective view illustrating a microplate in accordancewith some embodiments;

FIG. 4 is an enlarged perspective view illustrating a microplate inaccordance with some embodiments comprising a plurality of wellscomprising a circular rim portion;

FIG. 5 is an enlarged perspective view illustrating a microplate inaccordance with some embodiments comprising a plurality of wellscomprising a square-shaped rim portion;

FIG. 6 is a cross-sectional view illustrating a well comprising apressure relief bore according to some embodiments;

FIG. 7 is a cross-sectional view illustrating the well of FIG. 6 whereinthe pressure relief bore is partially filled;

FIG. 8 is a cross-sectional view illustrating a well comprising anoffset pressure relief bore according to some embodiments, being filledby a spotting device;

FIG. 9 is a cross-sectional view illustrating the well of FIG. 8 beingfilled by a micro-piezo dispenser;

FIG. 10 is a cross-sectional view illustrating a microplate employing aplurality of apertures, a backing sheet, and a sealing cover accordingto some embodiments;

FIG. 11 is a top view illustrating a microplate in accordance with someembodiments comprising one or more grooves;

FIG. 12 is an enlarged top view illustrating a corner of the microplateillustrated in FIG. 11;

FIG. 13 is a cross-sectional view of the microplate of FIG. 12 takenalong Line 13-13;

FIG. 14 is an enlarged top view illustrating a corner of a microplateaccording to some embodiments;

FIG. 15 is a cross-sectional view of the microplate of FIG. 14 takenalong Line 15-15;

FIG. 16 is a top view illustrating a microplate in accordance with someembodiments comprising at least one thermally isolated portion;

FIG. 17 is a side view illustrating the microplate of FIG. 16;

FIG. 18 is a bottom view illustrating the microplate of FIG. 16;

FIG. 19 is an enlarged cross-sectional view illustrating the microplateof FIG. 16 taken along Line 19-19;

FIG. 20 is an exploded perspective view illustrating a filling apparatusaccording to some embodiments;

FIG. 21 is a cross-sectional perspective view of the filling apparatusof FIG. 20;

FIG. 22( a) is a cross-sectional perspective view of a filling apparatusaccording to some embodiments;

FIG. 22( b) is a cross-sectional view of a portion of a fillingapparatus comprising a plurality of staging capillaries, microfluidicchannels, and ramp features according to some embodiments;

FIG. 23( a) is a top schematic view of a filling apparatus according tosome embodiments;

FIG. 23( b) is a top perspective view of a portion of a fillingapparatus comprising a plurality of staging capillaries, microfluidicchannels, and ramp features according to some embodiments;

FIG. 24 is a bottom perspective view of an output layer of a fillingapparatus comprising spacer features according to some embodiments;

FIGS. 25( a)-(f) are top schematic views of a filling apparatusaccording to some embodiments;

FIG. 26 is a cross-sectional view illustrating a well of a microplateaccording to some embodiments;

FIG. 27 is a cross-sectional view illustrating a well of an invertedmicroplate according to some embodiments;

FIG. 28 is a top perspective view illustrating a multipiece microplatein accordance with some embodiments;

FIG. 29 is an exploded perspective view illustrating the multipiecemicroplate of FIG. 28 in accordance with some embodiments;

FIG. 30 is a top view illustrating the multipiece microplate inaccordance with some embodiments;

FIG. 31 is a cross-sectional view of the multipiece microplate of FIG.30 taken along Line 31-31;

FIG. 32 is an enlarged cross-sectional view of cap portion and main bodyportion of the multipiece microplate of FIG. 31;

FIG. 33 is an exploded top perspective view illustrating a fillingapparatus comprising an intermediate layer according to someembodiments;

FIG. 34 is a cross-sectional view illustrating the filling apparatuscomprising the intermediate layer according to some embodiments;

FIG. 35 is an exploded bottom perspective view illustrating the fillingapparatus comprising the intermediate layer according to someembodiments;

FIG. 36 is a cross-sectional view illustrating the filling apparatuscomprising the intermediate layer and nodules according to someembodiments;

FIG. 37 is a top schematic view of the filling apparatus comprising theintermediate layer and nodules according to some embodiments;

FIG. 38 is a cross-sectional view illustrating the filling apparatuscomprising the intermediate layer, nodules, and sealing featureaccording to some embodiments;

FIG. 39 is a bottom perspective view of the intermediate layer of thefilling apparatus according to some embodiments;

FIG. 40 is an exploded top perspective view illustrating a clamp systemfor a filling apparatus according to some embodiments;

FIG. 41 is an exploded top perspective view illustrating a fillingapparatus comprising a vent layer according to some embodiments;

FIG. 42 is an exploded bottom perspective view illustrating the fillingapparatus comprising the vent layer according to some embodiments;

FIG. 43 is a cross-sectional view illustrating the filling apparatuscomprising the vent layer and a vent manifold according to someembodiments;

FIG. 44 is a top schematic view of the filling apparatus comprising thevent layer and circular vent apertures according to some embodiments;

FIG. 45 is a top schematic view of the filling apparatus comprising thevent layer and oblong vent apertures according to some embodiments;

FIG. 46 is a cross-sectional view illustrating the filling apparatuscomprising the vent layer and pressure bores according to someembodiments;

FIG. 47 is a perspective view illustrating a filling apparatuscomprising one or more assay input ports positioned on an end of aninput layer according to some embodiments;

FIG. 48 is a perspective view illustrating a filling apparatuscomprising one or more assay input ports positioned on a side of aninput layer according to some embodiments;

FIG. 49 is a perspective view illustrating a filling apparatuscomprising one or more assay input ports positioned on opposing sides ofan input layer according to some embodiments;

FIG. 50 is a perspective view with portions illustrated in cross-sectionillustrating an assay input port according to some embodiments;

FIG. 51 is a cross-sectional view illustrating the filling apparatus ofFIG. 50 according to some embodiments;

FIGS. 52-58 and 60 are cross-sectional views illustrating theprogressive filling of a microplate according to some embodiments;

FIG. 59 is a top schematic view of the filling apparatus comprisingreduced material areas for, at least in part, use in staking accordingto some embodiments;

FIGS. 61-66 are cross-sectional views illustrating the progressivefilling of a microplate using a filling apparatus employing fluidoverfill reservoirs according to some embodiments;

FIG. 67 is a cross-sectional view illustrating a filling apparatusemploying fluid overfill reservoirs disposed in an output layeraccording to some embodiments;

FIGS. 68( a)-(g) are top schematic views illustrating various possiblepositions of the staging capillaries relative to correspondingmicrofluidic channels according to some embodiments;

FIGS. 69( a)-(g) are cross-sectional views illustrating various possiblepositions and configurations microfluidic channels and stagingcapillaries according to some embodiments;

FIG. 70 is an exploded perspective view illustrating a filling apparatuscomprising a floating insert and cover according to some embodiments;

FIG. 71 is a cross-sectional view illustrating the filling apparatuscomprising the floating insert according to some embodiments;

FIG. 72 is an exploded perspective view illustrating a filling apparatuscomprising a floating insert according to some embodiments;

FIG. 73 is a cross-sectional view illustrating a floating insertaccording to some embodiments;

FIG. 74 is a cross-sectional view illustrating a floating insertcomprising post members according to some embodiments;

FIG. 75 is a cross-sectional view illustrating a floating insertcomprising tapered members according to some embodiments;

FIG. 76 is a cross-sectional view illustrating a floating insertcomprising tapered members and a flanged base portion according to someembodiments;

FIG. 77 is a cross-sectional view illustrating the floating insertcomprising tapered members and the flanged base portion inserted into acorresponding depression according to some embodiments;

FIG. 78 is a cross-sectional view illustrating the floating insertcomprising tapered members and the flanged base portion inserted intothe corresponding depression and assay flow therebetween according tosome embodiments;

FIG. 79 is a cross-sectional view illustrating the floating insertcomprising tapered members and the flanged base portion being forceddown onto the corresponding depression according to some embodiments;

FIGS. 80-82 are cross-sectional views illustrating the progressivefilling and release of assay from the filling apparatus illustrated inFIG. 72 according to some embodiments;

FIGS. 83 and 84 are cross-sectional views illustrating the filling andrelease of assay from a filling apparatus comprising weight membersaccording to some embodiments;

FIG. 85 is a perspective view illustrating a filling apparatuscomprising an output layer and reservoir pockets according to someembodiments;

FIG. 86 is a cross-sectional view illustrating the filling apparatuscomprising the output layer according to some embodiments;

FIGS. 87-89 are cross-sectional views illustrating the progressivefilling of a plurality of staging capillaries according to someembodiments;

FIG. 90 is a perspective view illustrating the filling apparatuscomprising the surface wire assembly, reservoir pockets, and absorbentmembers further comprising a sloping overflow channel portion accordingto some embodiments;

FIGS. 91-92 are perspective views illustrating the filling apparatuscomprising the surface wire assembly, the reservoir trough, andabsorbent member further comprising a sloping portion according to someembodiments;

FIG. 93 is a perspective view illustrating a filling apparatuscomprising a surface wire assembly, reservoir pockets, and absorbentmembers according to some embodiments;

FIG. 94 is a perspective view illustrating a funnel member comprising anassay chamber according to some embodiments;

FIG. 95 is a perspective view illustrating a funnel member comprisingmultiple discrete assay chambers according to some embodiments;

FIG. 96 is a perspective view illustrating a funnel member comprisingmultiple discrete assay chambers according to some embodiments;

FIG. 97 is a cross-sectional view illustrating a funnel membercomprising a tip portion according to some embodiments;

FIG. 98 is a cross-sectional view illustrating a funnel membercomprising a tip portion and a wiper member according to someembodiments;

FIG. 99 is a cross-sectional view illustrating a funnel membercomprising a tip portion and a planar cavity according to someembodiments;

FIG. 100 is a cross-sectional view illustrating a funnel membercomprising a tip portion and a wiper member spaced apart from the tipportion according to some embodiments;

FIG. 101 is a bottom perspective view illustrating a funnel membercomprising multiple offset discrete assay chambers according to someembodiments;

FIG. 102 is a top plan view illustrating a funnel member comprisingmultiple offset discrete assay chambers and one or more aperturesaccording to some embodiments;

FIG. 103 is a cross-sectional view illustrating a funnel membercomprising multiple offset discrete assay chambers and one or moreapertures according to some embodiments;

FIG. 104 is a top perspective view illustrating a multipiece funnelmember comprising multiple offset discrete assay chambers and aninternal siphon passage according to some embodiments;

FIG. 105 is a cross-sectional view illustrating the multipiece funnelmember comprising multiple offset discrete assay chambers and theinternal siphon passage according to some embodiments;

FIG. 106 is an exploded top perspective view illustrating a multipiecefunnel member comprising portions separated generally verticallyaccording to some embodiments;

FIG. 107 is an exploded bottom perspective view illustrating amultipiece funnel member comprising portions separated generallyhorizontally according to some embodiments;

FIG. 108 is an exploded top perspective view illustrating a fillingapparatus comprising an upwardly-shaped member according to someembodiments;

FIG. 109 is a top perspective view illustrating the filling apparatuscomprising the upwardly-shaped member according to some embodiments;

FIGS. 110-113 are cross-sectional views illustrating the progressivefilling of an output layer using in part a capillary plane according tosome embodiments;

FIGS. 114-119 are cross-sectional views illustrating the progressivefilling of an output layer using in part a capillary plane and wallrestraints according to some embodiments;

FIG. 120 is a top schematic view of a filling apparatus comprisingmicrofluidic channels arranged in a cross-pattern according to someembodiments;

FIG. 121 is a top perspective view of the filling apparatus comprisingmicrofluidic channels arranged in the cross-pattern according to someembodiments;

FIG. 122 is a top perspective view of a filling apparatus comprisingmicrofluidic channels arranged in an S-shaped pattern according to someembodiments;

FIG. 123 is a top schematic view of the filling apparatus comprisingmicrofluidic channels arranged in the S-shaped pattern according to someembodiments;

FIG. 124 is a top perspective view of a filling apparatus comprisingmicrofluidic channels arranged in an S-shaped pattern having wallrestraints according to some embodiments;

FIG. 125 is a top schematic view of the filling apparatus comprisingmicrofluidic channels arranged in the S-shaped pattern having wallrestraints according to some embodiments;

FIG. 126 is a top perspective view of a filling apparatus comprisingmicrofluidic channels arranged in an S-shaped pattern having wallrestraints extending from a side of a capillary plane according to someembodiments;

FIG. 127 is a top schematic view of the filling apparatus comprising theopen vent network according to some embodiments;

FIG. 128 is a top perspective view of a filling apparatus comprisingmicrofluidic channels arranged in a diagonal pattern according to someembodiments;

FIG. 129 is a top schematic view of the filling apparatus comprisingmicrofluidic channels arranged in the diagonal pattern according to someembodiments;

FIG. 130 is an enlarged, top perspective view of the filling apparatuscomprising microfluidic channels arranged in the diagonal patternaccording to some embodiments;

FIG. 131 is an enlarged, top perspective view of a filling apparatuscomprising microfluidic channels arranged in an H-shaped patternaccording to some embodiments;

FIG. 132 is a top schematic view of the filling apparatus comprisingmicrofluidic channels arranged in the H-shaped pattern according to someembodiments;

FIG. 133 is an enlarged, top perspective view of a filling apparatuscomprising microfluidic channels arranged in one or more S-shapedpatterns according to some embodiments;

FIG. 134 is a top schematic view of the filling apparatus comprisingmicrofluidic channels arranged in one or more S-shaped patternsaccording to some embodiments;

FIG. 135 is an enlarged, top perspective view of the filling apparatuscomprising microfluidic channels arranged in one or more S-shapedpatterns according to some embodiments;

FIG. 136 is a top perspective view of a centrifuge during initialacceleration;

FIG. 137 is a top perspective view of the centrifuge during steady stateoperation;

FIG. 138 is an exploded top perspective view illustrating a fillingapparatus comprising an open vent network according to some embodiments;

FIG. 139 is a top perspective view illustrating the filling apparatuscomprising the open vent network according to some embodiments;

FIG. 140 is a top perspective view of the filling apparatus comprisingthe open vent network during an initial filling step according to someembodiments;

FIGS. 141-143 are top schematic views illustrating the progressivefilling of the filling apparatus comprising the open vent networkaccording to some embodiments;

FIG. 144 is a top schematic view illustrating a filling apparatuscomprising delay-filled capillaries according to some embodiments;

FIGS. 145-148 are cross-sectional views illustrating the progressivefilling of the filling apparatus comprising delay-filled capillariesaccording to some embodiments;

FIG. 149 is a top perspective view illustrating a filling apparatuscomprising delay-filled channels according to some embodiments;

FIG. 150 is a top perspective view illustrating a filling apparatuscomprising an overflow moat according to some embodiments;

FIGS. 151-152 are cross-sectional views illustrating the progressivefilling of the filling apparatus comprising the overflow moat accordingto some embodiments;

FIG. 153 is a cross-sectional view illustrating a filling apparatuscomprising burst pockets according to some embodiments;

FIG. 154 is an exploded top perspective view illustrating the fillingapparatus comprising burst pockets according to some embodiments;

FIGS. 155-157 are top schematic views illustrating the burst pocketsprior to centrifugation according to some embodiments;

FIGS. 158-160 are top schematic views illustrating the burst pocketsafter centrifugation according to some embodiments;

FIG. 161 is a top perspective view illustrating a filling apparatuscomprising a sweep loader system according to some embodiments;

FIG. 162 is a top perspective view illustrating a microplate for usewith the filling apparatus comprising the sweep loader system accordingto some embodiments;

FIG. 163 is an enlarged top perspective view illustrating the microplateaccording to some embodiments;

FIG. 164 is a top perspective view illustrating the sweep loaderaccording to some embodiments;

FIG. 165 is a side perspective view illustrating a wedge elevator of thesweep loader in a lowered position according to some embodiments;

FIG. 166 is a side perspective view illustrating the wedge elevator ofthe sweep loader in a raised position according to some embodiments;

FIG. 167 is a top perspective view illustrating the sweep loader in araised position according to some embodiments;

FIG. 168 is a bottom perspective view, with portions in cross-section,illustrating the sweep loader in the raised position according to someembodiments; and

FIG. 169 is a top perspective view illustrating a microplate for usewith the filling apparatus comprising the sweep loader system accordingto some embodiments.

FIG. 170 is a cross-sectional view illustrating a filling apparatuscomprising a porous material member according to some embodiments;

FIG. 171 is a cross-sectional view illustrating a filling apparatuscomprising a hydrophobic feature disposed between staging capillariesaccording to some embodiments;

FIG. 172 is a cross-sectional view illustrating a filling apparatuscomprising the hydrophobic feature aligned with staging capillariesaccording to some embodiments;

DESCRIPTION OF SOME EMBODIMENTS

The following description of some embodiments is merely exemplary innature and is in no way intended to limit the present teachings,applications, or uses. Although the present teachings will be discussedin some embodiments as relating to polynucleotide amplification, such asPCR, such discussion should not be regarded as limiting the presentteaching to only such applications.

The section headings and sub-headings used herein are for generalorganizational purposes only and are not to be construed as limiting thesubject matter described in any way.

High-Density Sequence Detection System

In some embodiments, a high density sequence detection system comprisesone or more components useful in an analytical method or chemicalreaction, such as the analysis of biological and other materialscontaining polynucleotides. Such systems are, in some embodiments,useful in the analysis of assays, as further described below. Highdensity sequence detection systems, in some embodiments, comprise anexcitation system and a detection system which can be useful foranalytical methods involving the generation and/or detection ofelectromagnetic radiation (e.g., visible, ultraviolet or infrared light)generated during analytical procedures. In some embodiments, suchprocedures include those comprising the use of fluorescent or othermaterials that absorb and/or emit light or other radiation underconditions that allow quantitative and/or qualitative analysis of amaterial (e.g., assays among those described herein). In someembodiments useful for polynucleotide amplification and/or detection, ahigh density sequence detection system can further comprise athermocycler. In some embodiments, a high density sequence system canfurther comprise microplate and components for, e.g., filling andhandling the microplate, such as a pressure clamp system. It will beunderstood that, although high density sequence detection systems aredescribed herein with respect to specific microplates, assays and otherembodiments, such systems and components thereof are useful with avariety of analytical platforms, equipment, and procedures.

Referring to FIG. 1, a high-density sequence detection system 10 isillustrated in accordance with some embodiments of the presentteachings. In some embodiments, high-density sequence detection system10 comprises a microplate 20 containing an assay 1000 (see FIGS. 26 and27), a thermocycler system 100, a pressure clamp system 110, anexcitation system 200, and a detection system 300 disposed in a housing1008.

In some embodiments, assay 1000 can comprise any material that is usefulin, the subject of, a precursor to, or a product of, an analyticalmethod or chemical reaction. In some embodiments for amplificationand/or detection of polynucleotides, assay 1000 comprises one or morereagents (such as PCR master mix, as described further herein); ananalyte (such as a biological sample comprising DNA, a DNA fragment,cDNA, RNA, or any other nucleic acid sequence), one or more primers, oneor more primer sets, one or more detection probes; components thereof;and combinations thereof. In some embodiments, assay 1000 comprises ahomogenous solution of a DNA sample, at least one primer set, at leastone detection probe, a polymerase, and a buffer, as used in a homogenousassay (described further herein). In some embodiments, assay 1000 cancomprise an aqueous solution of at least one analyte, at least oneprimer set, at least one detection probe, and a polymerase. In someembodiments, assay 1000 can be an aqueous homogenous solution. In someembodiments, assay 1000 can comprise at least one of a plurality ofdifferent detection probes and/or primer sets to perform multiplex PCR,which can be useful, for example, when analyzing a whole genome (e.g.,20,000 to 30,000 genes, or more) or other large numbers of genes or setsof genes.

Microplate

In some embodiments, a microplate comprises a substrate useful in theperformance of an analytical method or chemical reaction. In someembodiments, the microplate is substantially planar, havingsubstantially planar upper and lower surfaces, wherein the dimensions ofthe planar surfaces in the x- and y-dimensions are substantially greaterthan the thickness of the substrate in the z-direction. In someembodiments, a microplate can comprise one or more material retentionregions or reaction chambers, configured to hold or support a material(e.g., an assay, as discussed below, or other solid or liquid) at one ormore locations on or in the microplate. In some embodiments, suchmaterial retention regions can be wells, through-holes, reaction spotsor pads, and the like. In some embodiments, such as shown in FIGS. 2-19,material retention regions comprise wells 26. In some embodiments, wells26 can comprise a feature on or in the surface of the microplate whereinassay 1000 is contained at least in part by physical separation fromadjacent features. Such well features can include, in some embodiments,depressions, indentations, ridges, and combinations thereof, in regularor irregular shapes. In some embodiments a microplate is single-use,wherein it is filled or otherwise used with a single assay for a singleexperiment or set of experiments, and is thereafter discarded. In someembodiments, a microplate is multiple-use, wherein it can be operablefor use in a plurality of experiments or sets of experiments.

Referring now to FIGS. 2-19, in some embodiments, microplate 20comprises a substantially planar construction having a first surface 22and an opposing second surface 24 (see FIGS. 12-19). First surface 22comprises a plurality of wells 26 disposed therein or thereon. Theoverall positioning of the plurality of wells 26 can be referred to as awell array. Each of the plurality of wells 26 is sized to receive assay1000 (FIGS. 26 and 27). As illustrated in FIGS. 26 and 27, assay 1000 isdisposed in at least one of the plurality of wells 26 and sealing cover80 (FIG. 26) is disposed thereon (as will be discussed herein). In someembodiments, one or more of the plurality of wells 26 may not becompletely filled with assay 1000, thereby defining a headspace 1006(FIG. 26), which can define an air gap or other gas gap.

In some embodiments, the material retention regions of microplate 20 cancomprise a plurality of reaction spots on the surface of the microplate.In such embodiments, a reaction spot can be an area on the microplatewhich localizes, at least in part by non-physical means, assay 1000. Insuch embodiments, assay 1000 can be localized in sufficient quantity,and isolation from adjacent areas on the microplate, so as to facilitatean analytical or chemical reaction (e.g., amplification of one or moretarget DNA) in the material retention region. Such localization can beaccomplished by physical and chemical modalities, including, forexample, physical containment of reagents in one dimension and chemicalcontainment in one or more other dimensions.

Microplate Footprint

With reference to FIGS. 2-19, microplate 20 generally comprises a mainbody or substrate 28. In some embodiments, main body 28 is substantiallyplanar. In some embodiments, microplate 20 comprises an optional skirtor flange portion 30 disposed about a periphery of main body 28 (seeFIG. 2). Skirt portion 30 can form a lip around main body 28 and canvary in height. Skirt portion 30 can facilitate alignment of microplate20 on thermocycler block 102. Additionally, skirt portion 30 can provideadditional rigidity to microplate 20 such that during handling, filling,testing, and the like, microplate 20 remains rigid, thereby ensuringassay 1000, or any other components, disposed in each of the pluralityof wells 26 does not contaminate adjacent wells. However, in someembodiments, microplate 20 can employ a skirtless design (see FIGS. 3-5)depending upon user preference.

In some embodiments, microplate 20 can be from about 50 to about 200 mmin width, and from about 50 to about 200 mm in length. In someembodiments, microplate 20 can be from about 50 to about 100 mm inwidth, and from about 100 to about 150 mm in length. In someembodiments, microplate 20 can be about 72 mm wide and about 120 mmlong.

In order to facilitate use with existing equipment, robotic implements,and instrumentation, the footprint dimensions of main body 28 and/orskirt portion 30 of microplate 20, in some embodiments, can conform tostandards specified by the Society of Biomolecular Screening (SBS) andthe American National Standards Institute (ANSI), published January 2004(ANSI/SBS 3-2004). In some embodiments, the footprint dimensions of mainbody 28 and/or skirt portion 30 of microplate 20 are about 127.76 mm(5.0299 inches) in length and about 85.48 mm (3.3654 inches) in width.In some embodiments, the outside corners of microplate 20 comprise acorner radius of about 3.18 mm (0.1252 inches). In some embodiments,microplate 20 comprises a thickness of about 0.5 mm to about 3.0 mm. Insome embodiments, microplate 20 comprises a thickness of about 1.25 mm.In some embodiments, microplate 20 comprises a thickness of about 2.25mm. One skilled in the art will recognize that microplate 20 and skirtportion 30 can be formed in dimensions other than those specifiedherein.

Plurality of Material Retention Regions

The density of material retention regions (i.e., number of materialretention regions per unit surface area of microplate) and the size andvolume of material retention regions can vary depending on the desiredapplication and such factors as, for example, the species of theorganism for which the methods of the present teachings may be employed.In some embodiments, the density of material retention regions can befrom about 10 to about 1000 regions/cm², or from about 50 to about 100regions/cm², for example about 79 regions/cm². In some embodiments, thedensity of material retention regions can be from about 150 to about 170regions/cm². In some embodiments, the density of material retentionregions can be from about 480 to about 500 regions/cm².

In some embodiments, the pitch of material retention regions onmicroplate 20 can be from about 50 to about 10000 μm, or from about 50to about 1500 μm, or from about 450 to 550 μm. In some embodiments, thepitch of material retention regions on microplate 20 can be from about50 to about 1000 μm, or from about 400 to 500 μm. In some embodiments,the pitch can be from about 1000 to 1200 μm. In some embodiments, thedistance between the material retention regions (the thickness of thewall between chambers) can be from about 50 to about 200 μm, or fromabout 100 to about 200 μm, for example, about 150 μm.

In some embodiments, the total number of material retention regions onthe microplate can be from about 5000 to about 100,000, or from about5000 to about 50,000, or from about 5000 to about 10,000. In someembodiments, the microplate can comprise from about 10,000 to about15,000 material retention regions. In some embodiments, the microplatecan comprise from about 25,000 to about 35,000 material retentionregions.

In order to increase throughput of genotyping, gene expression, andother assays, in some embodiments, microplate 20 comprises an increasedquantity of the plurality of wells 26 beyond that employed in priorconventional microplates. In some embodiments, microplate 20 comprises6,144 wells. According to the present teachings, microplate 20 cancomprise, but is not limited to, any of the array configurations ofwells described in Table 1.

TABLE 1 Total Number of Wells Rows × Columns Approximate Well Area 96  8× 12 9 × 9 mm 384 16 × 24 4.5 × 4.5 mm 1536 32 × 48 2.25 × 2.25 mm 345648 × 72 1.5 × 1.5 mm 6144 64 × 96 1.125 × 1.125 mm 13824  96 × 144 0.75× .075 mm 24576 128 × 192 0.5625 × 0.5625 mm 55296 192 × 288 0.375 ×0.375 mm 768 24 × 32 3 × 3 mm 1024 32 × 32 2.25 × 3 mm 1600 40 × 40 1.8× 2.7 mm 1280 32 × 40 2.25 × 2.7 mm 1792 32 × 56 2.25 × 1.714 mm 2240 40× 56 1.8 × 1.714 mm 864 24 × 36 3 × 3 mm 4704 56 × 84 1.257 × 1.257 mm7776  72 × 108 1 × 1 mm 9600  80 × 120 0.9 × .09 mm 11616  88 × 1320.818 × 0.818 mm 16224 104 × 156 0.692 × 0.692 mm 18816 112 × 168 0.643× 0.643 mm 21600 120 × 180 0.6 × 0.6 mm 27744 136 × 204 0.529 × 0.529 mm31104 144 × 216 0.5 × 0.5 mm 34656 152 × 228 0.474 × 0.474 mm 38400 160× 240 0.45 × 0.45 mm 42336 168 × 252 0.429 × 0.429 mm 46464 176 × 2640.409 × 0.409 mm 50784 184 × 256 0.391 × 0.391 mmMaterial Retention Region Size and Shape

According to some embodiments, as illustrated in FIGS. 4 and 5, each ofthe plurality of material retention regions (e.g., wells 26) can besubstantially equivalent in size. The plurality of wells 26 can have anycross-sectional shape. In some embodiments, as illustrated in FIGS. 4,26, and 27, each of the plurality of wells 26 comprises a generallycircular rim portion 32 (FIG. 4) with a downwardly-extending,generally-continuous sidewall 34 that terminate at a bottom wall 36interconnected to sidewall 34 with a radius. A draft angle of sidewall34 can be used in some embodiments. In some embodiments, the draft angleprovides benefits including increased ease of manufacturing andminimizing shadowing (as discussed herein). The particular draft angleis determined, at least in part, by the manufacturing method and thesize of each of the plurality of wells 26. In some embodiments, circularrim portion 32 can be about 1.0 mm in diameter, the depth of each of theplurality of wells 26 can be about 0.9 mm, the draft angle of sidewall34 can be about 1° to 5° or greater and each of the plurality of wells26 can have a center-to-center distance of about 1.125 mm. In someembodiments, the volume of each of the plurality of wells 26 can beabout 500 nanoliters.

According to some embodiments, as illustrated in FIG. 5, each of theplurality of wells 26 comprises a generally square-shaped rim portion 38with downwardly-extending sidewalls 40 that terminate at a bottom wall42. A draft angle of sidewalls 40 can be used. Again, the particulardraft angle is determined, at least in part, by the manufacturing methodand the size of each of the plurality of wells 26. In some embodimentsof wells 26 of FIG. 5, generally square-shaped rim portion 38 can have aside dimension of about 1.0 mm in length, a depth of about 0.9 mm, adraft angle of about 1° to 5° or greater, and a center-to-centerdistance of about 1.125 mm, generally indicated at A (see FIG. 27). Insome embodiments, the volume of each of the plurality of wells 26 ofFIG. 5 can be about 500 nanoliters. In some embodiments, the spacingbetween adjacent wells 26, as measured at the top of a wall dividing thewells, is less than about 0.5 m. In some embodiments, this spacingbetween adjacent wells 26 is about 0.25 mm.

In some embodiments, and in some configurations, the plurality of wells26 comprising a generally circular rim portion 32 can provide advantagesover the plurality of wells 26 comprising a generally square-shaped rimportion 38. In some embodiments, during heating, it has been found thatassay 1000 can migrate through capillary action upward along edges ofsidewalls 40. This can draw assay 1000 from the center of each of theplurality of wells 26, thereby causing variation in the depth of assay1000. Variations in the depth of assay 1000 can influence the emissionoutput of assay 1000 during analysis. Additionally, during manufactureof microplate 20, in some cases cylindrically shaped mold pins used toform the plurality of wells 26 comprising generally circular rim portion32 can permit unencumbered flow of molten polymer thereabout. Thisunencumbered flow of molten polymer results in less deleterious polymermolecule orientation. In some embodiments, generally circular rimportion 32 provides more surface area along microplate 20 for improvedsealing with sealing cover 80, as is discussed herein.

In some embodiments, the area of each material retention region can befrom about 0.01 to about 0.05 mm². In some embodiments, the width ofeach material retention region can be from about 200 to about 2,000microns, or from about 800 to about 3000 microns. In some embodiments,the depth of each material retention region can be about 1100 microns,or about 850 microns. In some embodiments, the surface area of eachmaterial retention region can be from about 0.01 to about 0.05 mm², orfrom about 0.02 to about 0.04 mm². In some embodiments, the aspect ratio(ratio of depth:width) of each material retention region can be fromabout 1 to about 4, or about 2.

In some embodiments, the volume of the material retention regions can beless than about 50 μl, or less than about 10 μl. In some embodiments,the volume can be from about 0.05 to about 500 nanoliters, from about0.1 to about 200 nanoliters, from about 20 to about 150 nanoliters, fromabout 80 to about 120 nanoliters, from about 50 to about 100 nanoliters,from about 1 to about 5 nanoliters, or less than about 2 nanoliters.

Through-Hole Material Retention Regions

As illustrated in FIG. 10, in some embodiments, each of the materialretention regions of microplate 20 can comprise a plurality of apertures48 being sealed at least on one end by sealing cover 80. In someembodiments, each of the plurality of apertures 48 can be sealed on anopposing end with a backing sheet 50, which can have a clear or opaqueadhesive. In some embodiments, backing sheet 50 can comprise a heatconducting material such as, for example, a metal foil or a metal coatedplastic. In some embodiments, backing sheet 50 can be placed againstthermocycler block 102 to aid in thermal conductivity and distribution.In some embodiments, backing sheet 50 can comprise a plurality ofreaction spots (as discussed herein), coated on discrete areas of thesurface of backing sheet 50, such that in some circumstances theplurality of reaction spots can be aligned with the plurality ofapertures 48.

In some embodiments, a layer of mineral oil can be placed at the top ofeach of the plurality of apertures 48 before, or as an alternative to,placement of sealing cover 80 on microplate 20. In several of suchembodiments, the mineral oil can fill a portion of each of the pluralityof apertures 48 and provide an optical interface and can controlevaporation of assay 1000.

Pressure Relief Bores

Referring now to FIGS. 6-9, in some embodiments, each of the pluralityof wells 26 of microplate 20 can comprise a pressure relief bore 44. Insome embodiments, pressure relief bore 44 is sized such that it does notinitially fill with assay 1000 due to surface tension. However, whenassay 1000 is heated during thermocycling, assay 1000 expands, therebyincreasing an internal fluid pressure in each of the plurality of wells26. This increased internal fluid pressure is sufficient to permit assay1000 to flow into pressure relief bore 44 as illustrated in FIG. 7,thereby minimizing the pressure exerted on sealing cover 80. In someembodiments, each of the plurality of wells 26 can have one or aplurality of pressure relief bores 44.

In some embodiments, as illustrated in FIGS. 8 and 9, pressure reliefbore 44 can be offset within each of the plurality of wells 26 so thateach of the plurality of wells 26 can be filled with assay 1000 or othermaterial 1004 via a spotting device 700 (FIG. 8) or a micro-piezodispenser 702 (FIG. 9). In some embodiments, a top edge 46 of pressurerelief bore 44 can be generally square and have minimal or no radius.This arrangement can reduce the likelihood that assay 1000 or othermaterial 1004 will enter pressure relief bore 44 prior to thermocycling.

Grooves

Referring to FIGS. 11-15, in some embodiments, microplate 20 cancomprise grooves 52 and grooves 54 disposed about a periphery of theplurality of wells 26. In some embodiments, grooves 52 can have depthand width dimensions generally similar to the depth and width dimensionsof the plurality of wells 26 (FIGS. 12 and 13). In some embodiments,grooves 54 can have depth and width dimensions less than the depth andwidth dimensions of the plurality of wells 26 (FIGS. 14 and 15). In someembodiments, as illustrated in FIG. 12, additional grooves 56 can bedisposed at opposing sides of microplate 20. In some embodiments,grooves 52, 54, and 56 can improve thermal uniformity among theplurality of wells 26 in microplate 20. In some embodiments, grooves 52,54, and 56 can improve the sealing interface formed by sealing cover 80and microplate 20. Grooves 52, 54, and 56 can also assist in simplifyingthe injection molding process of microplate 20. In some embodiments, aliquid solution similar to assay 1000 can be disposed in grooves 52, 54,and 56 to, in part, improve thermal uniformity during thermocycling.

Alignment Features

In some embodiments, as illustrated in FIGS. 2, 3, 11, and 14,microplate 20 comprises an alignment feature 58, such as a cornerchamfer, a pin, a slot, a cut corner, an indentation, a graphic, orother unique feature that is capable of interfacing with a correspondingfeature formed in a fixture, reagent dispensing equipment, and/orthermocycler. In some embodiments, alignment feature 58 comprises a nubor protrusion 60 as illustrated in FIG. 14. Additionally, in someembodiments, alignment features 58 are placed such that they do notinterfere with sealing cover 80 or at least one of the plurality ofwells 26. However, locating alignment features 58 near at least one ofthe plurality of wells 26 can provide improved alignment with dispensingequipment and/or thermocycler block 102.

Thermally Isolated Portion

In some embodiments, as illustrated in FIGS. 16-19, microplate 20comprises a thermally isolated portion 62. Thermally isolated portion 62can be disposed along at least one edge of main body 28. Thermallyisolated portion 62 can be generally free of wells 26 and can be sizedto receive a marking indicia 64 (discussed in detail herein) thereon.Thermally isolated portion 62 can further be sized to facilitate thehandling of microplate 20 by providing an area that can be easilygripped by a user or mechanical device without disrupting the pluralityof wells 26.

Still referring to FIGS. 16-19, in some embodiments, microplate 20comprises a first groove 66 formed along first surface 22 and a secondgroove 68 formed along an opposing second surface 24 of microplate 20.First groove 66 and second groove 68 can be aligned with respect to eachother to extend generally across microplate 20 from a first side 70 to asecond side 72. First groove 66 and second groove 68 can be furtheraligned upon first surface 22 and second surface 24 to define a reducedcross-section 74 between thermally isolated portion 62 and the pluralityof wells 26. This reduced cross-section 74 can provide a thermalisolation barrier to reduce any heat sink effect introduced by thermallyisolated portion 62, which might otherwise reduce the temperature cycleof some of the plurality of wells 26.

Marking Indicia

In some embodiments, as illustrated in FIGS. 2, 16 and 17, microplate 20comprises marking indicia 64, such as graphics, printing, lithograph,pictorial representations, symbols, bar codes, handwritings or any othertype of writing, drawings, etchings, indentations, embossments or raisedmarks, machine readable codes (i.e. bar codes, etc.), text, logos,colors, and the like. In some embodiments, marking indicia 64 ispermanent.

In some embodiments, marking indicia 64 can be printed upon microplate20 using any known printing system, such as inkjet printing, padprinting, hot stamping, and the like. In some embodiments, such as thoseusing a light-colored microplate 20, a dark ink can be used to createmarking indicia 64 or vice versa.

In some embodiments, microplate 20 can be made of polypropylene and havea surface treatment applied thereto to facilitate applying markingindicia 64. In some embodiments, such surface treatment comprises flametreatment, corona treatment, treating with a surface primer, or acidwashing. However, in some embodiments, a UV-curable ink can be used forprinting on polypropylene microplates.

Still further, in some embodiments, marking indicia 64 can be printedupon microplate 20 using a CO₂ laser marking system. Laser markingsystems evaporate material from a surface of microplate 20. Because CO₂laser etching can produce reduced color changes of marking indicia 64relative to the remaining portions of microplate 20, in someembodiments, a YAG laser system can be used to provide improved contrastand reduced material deformation.

In some embodiments, a laser activated pigment can be added to thematerial used to form microplate 20 to obtain improved contrast betweenmarking indicia 64 and main body 28. In some embodiments, anantimony-doped tin oxide pigment can be used, which is easily dispersedin polymers and has marking speeds as high as 190 inches per second.Antimony-doped tin oxide pigments can absorb laser light and can convertlaser energy to thermal energy in embodiments where indicia are createdusing a YAG laser.

In some embodiments, marking indicia 64 can identify microplates 20 tofacilitate identification during processing. Furthermore, in someembodiments, marking indicia 64 can facilitate data collection so thatmicroplates 20 can be positively identified to properly correlateacquired data with the corresponding assay. Such marking indicia 64 canbe employed as part of Good Laboratory Practices (GLP) and GoodManufacturing Practices (GMP), and can further, in some circumstances,reduce labor associated with manually applying adhesive labels, manuallytracking microplates, and correlating data associated with a particularmicroplate.

In some embodiments, marking indicia 64 can assist in alignment byplacing a symbol or other machine-readable graphic on microplate 20. Anoptical sensor or optical eye can detect marking indicia 64 and candetermine a location of microplate 20. In some embodiments, suchlocation of microplate 20 can then be adjusted to achieve apredetermined position using, for example, a drive system ofhigh-density sequence detection system 10, sealing cover applicator1100, or other corresponding systems.

In some embodiments, the type (physical properties, characteristics,etc.) of marking indicia employed on a microplate can be selected so asto reduce thermal and/or chemical interference during thermocyclingrelative to what might otherwise occur with other types of markingindicia (e.g., common prior indicia designs, such as adhesive labels).For example, adhesive labels can, in some circumstances, interfere(e.g., chemically interact) with one or more reagents (e.g., dyes) beingused.

Referring to FIG. 2, in some embodiments, a radio frequencyidentification (RFID) tag 76 can be used to electronically identifymicroplate 20. RFID tag 76 can be attached or molded within microplate20. An RFID reader (not illustrated) can be integrated into high-densitysequence detection system 10 to automatically read a uniqueidentification and/or data handling parameters of microplate 20.Further, RFID tag 76 does not require line-of-sight for readability. Itshould be appreciated that RFID tag 76 can be variously configured andused according to various techniques, such as those described incommonly-assigned U.S. patent application Ser. No. 11/086,069, entitled“SAMPLE CARRIER DEVICE INCORPORATING RADIO FREQUENCY IDENTIFICATION, ANDMETHOD” filed herewith.

Multi-Piece Construction

In some embodiments, such as illustrated in FIGS. 28-32, microplate 20can comprise a multi-piece construction. In some embodiments, microplate20 can comprise main body 28 and a separate cap portion 95 that can beconnected with main body 28. In some embodiments, cap portion 95 can besized and/or shaped to mate with main body 28 such that the combinationthereof results in a footprint that conforms to the above-described SBSand/or ANSI standards. Alternatively, main body 28 and/or cap portion 95can comprise non-standard dimensions, as desired.

Cap portion 95 can be coupled with main body 28 in a variety of ways. Insome embodiments, cap portion 95 comprises a cavity 96 (FIG. 32), suchas a mortis, sized and/or shaped to receive a support member 97, such asa tenon, extending from main body 28 to couple cap portion 95 with mainbody 28. In some embodiments, cavity 96 of cap portion 95 and supportmember 97 of main body 28 can comprise an interference fit or otherlocking feature, such as a hook member, to at least temporarily joinmain body 28 and cap portion 95 during assembly. In some embodiments,support member 97 of main body 28 can comprise a cap alignment feature98 that can interface with a corresponding feature 99 on cap portion 95to properly align cap portion 95 relative to main body 28. In someembodiments, cap portion 95 can comprise alignment feature 58 for use inlater alignment of microplate 20 as described herein. In someembodiments, alignment feature 58 can be disposed on main body 28 toreduce tolerance buildup caused by the interface of cap portion 95 andmain body 28.

In some embodiments, cap portion 95 can be formed directly on main body28, such as through over-molding. In such embodiments, main body 28 canbe placed within a mold cavity that generally closely conforms to mainbody 28 and defines a cap portion cavity generally surrounding supportmember 97 of main body 28. Over-molding material can then be introducedabout support member 97 within cap portion cavity to form cap portion 95thereon.

In some embodiments, cap portion 95 comprises marking indicia 64 on anysurface(s) thereon (e.g. top surface, bottom surface, side surface). Insome embodiments, cap portion 95 can comprise an enlarged print areathereon relative to embodiments employing first groove 66 (FIG. 16-19).In some embodiments, cap portion 95 can be made of a material differentfrom main body 28. In some embodiments, cap portion 95 can be made of amaterial that is particularly conducive to a desired form of printing ormarking, such as through laser marking. In some embodiments, alaser-activated pigment can be added to the material used to form capportion 95 to obtain improved contrast between marking indicia 64 andcap portion 95. In some embodiments, an antimony-doped tin oxide pigmentcan be used. In some embodiments, cap portion 95 can be color-coded toaid in identifying a particular microplate relative to others.

In some embodiments, cap portion 95 can serve to provide a thermalisolation barrier through the interface of cavity member 96 and supportmember 97 to reduce any heat sink effect of cap portion 95 relative tomain body 28 to maintain a generally consistent temperature cycle of theplurality of wells 26. Cap portion 95 can be made, for example, of anon-thermally conductive material, such as one or more of those setforth herein, to, at least in part, help to thermally isolate capportion 95 from main body 28.

In some embodiments, cap portion 95 can serve to conceal any injectionmolding gates coupled to support member 97 during molding. Duringmanufacturing, as such gates are removed from any product, aestheticvariations can result. Any such aesthetic variations in main body 28 canbe concealed in some embodiments using cap portion 95. In some case,injection-molding gates can lead to a localized increase influorescence. In some embodiments, such localized increase influorescence can be reduced using cap portion 95.

Microplate Material

In some embodiments, microplate 20 can comprise, at least in part, athermally conductive material. In some embodiments, a microplate, inaccordance with the present teachings, can be molded, at least in part,of a thermally conductive material to define a cross-plane thermalconductivity of at least about 0.30 W/mK or, in some embodiments, atleast about 0.58 W/mK. Such thermally conductive materials can provide avariety of benefits, such as, in some cases, improved heat distributionthroughout microplate 20, so as to afford reliable and consistentheating and/or cooling of assay 1000. In some embodiments, thisthermally conductive material comprises a plastic formulated forincreased thermal conductivity. Such thermally conductive materials cancomprise, for example and without limitation, at least one ofpolypropylene, polystyrene, polyethylene, polyethyleneterephthalate,styrene, acrylonitrile, cyclic polyolefin, syndiotactic polystyrene,polycarbonate, liquid crystal polymer, conductive fillers or plasticmaterials; and mixtures or combinations thereof. In some embodiments,such thermally conductive materials include those known to those skilledin the art with a melting point greater than about 130° C. For example,microplate 20 can be made of commercially available materials such asRTP199X104849, COOLPOLY E1201, or, in some embodiments, a mixture ofabout 80% RTP199X104849 and 20% polypropylene.

In some embodiments, microplate 20 can comprise at least one carbonfiller, such as carbon, graphite, impervious graphite, and mixtures orcombinations thereof. In some cases, graphite has an advantage of beingreadily and cheaply available in a variety of shapes and sizes. Oneskilled in the art will recognize that impervious graphite can benon-porous and solvent-resistant. Progressively refined grades ofgraphite or impervious graphite can provide, in some cases, a moreconsistent thermal conductivity.

In some embodiments, one or more thermally conductive ceramic fillerscan be used, at least in part, to form microplate 20. In someembodiments, the thermally conductive ceramic fillers can comprise boronnitrate, boron nitride, boron carbide, silicon nitride, aluminumnitride, and mixtures or combinations thereof.

In some embodiments, microplate 20 can comprise an inert thermallyconductive coating. In some embodiments, such coatings can includemetals or metal oxides, such as copper, nickel, steel, silver, platinum,gold, copper, iron, titanium, alumina, magnesium oxide, zinc oxide,titanium oxide, and mixtures thereof.

In some embodiments, microplate 20 comprises a mixture of a thermallyconductive material and other materials, such as non-thermallyconductive materials or insulators. In some embodiments, thenon-thermally conductive material comprises glass, ceramic, silicon,standard plastic, or a plastic compound, such as a resin or polymer, andmixtures thereof to define a cross-plane thermal conductivity of belowabout 0.30 W/mK. In some embodiments, the thermally conductive materialcan be mixed with liquid crystal polymers (LCP), such as wholly aromaticpolyesters, aromatic-aliphatic polyesters, wholly aromaticpoly(ester-amides), aromatic-aliphatic poly(ester-amides), aromaticpolyazomethines, aromatic polyester-carbonates, and mixtures thereof. Insome embodiments, the composition of microplate 20 can comprise fromabout 30% to about 60%, or from about 38% to about 48% by weight, of thethermally conductive material.

The thermally conductive material and/or non-thermally conductivematerial can be in the form of, for example, powder particles, granularpowder, whiskers, flakes, fibers, nanotubes, plates, rice, strands,hexagonal or spherical-like shapes, or any combination thereof. In someembodiments, the microplate comprises thermally conductive additiveshaving different shapes to contribute to an overall thermal conductivitythat is higher than any one of the individual additives alone.

In some embodiments, the thermally conductive material comprises apowder. In some embodiments, the particle size used herein can bebetween 0.10 micron and 300 microns. When mixed homogeneously with aresin in some embodiments, powders provide uniform (i.e. isotropic)thermal conductivity in all directions throughout the composition of themicroplate.

As discussed above, in some embodiments, the thermally conductivematerial can be in the form of flakes. In some such embodiments, theflakes can be irregularly shaped particles produced by, for example,rough grinding to a desired mesh size or the size of mesh through whichthe flakes can pass. In some embodiments, the flake size can be between1 micron and 200 microns. Homogenous compositions containing flakes can,in some cases, provide uniform thermal conductivity in all directions.

In some embodiments, the thermally conductive material can be in theform of fibers, also known as rods. Fibers can be described, among otherways, by their lengths and diameters. In some embodiments, the length ofthe fibers can be, for example, between 2 mm and 15 mm. The diameter ofthe fibers can be, for example, between 1 mm and 5 mm. Formulations thatinclude fibers in the composition can, in some cases, have the benefitof reinforcing the resin for improved material strength.

In some embodiments, microplate 20 can comprise a material comprisingadditives to promote other desirable properties. In some embodiments,these additives can comprise flame-retardants, antioxidants,plasticizers, dispersing aids, marking additives, and mold-releasingagents. In some embodiments, such additives are biologically and/orchemically inert.

In some embodiments, microplate 20 comprises, at least in part, anelectrically conductive material, which can improve reagent dispensingalignment. In this regard, electrically conductive material can reducestatic build-up on microplate 20 so that the reagent droplets will notgo astray during dispensing. In some embodiments, a voltage can beapplied to microplate 20 to pull the reagent droplets into apredetermined position, particularly with a co-molded part where thebottom section can be electrically conductive and the sides of theplurality of wells 26 may not be electrically conductive. In someembodiments, a voltage field applied to the electrically conductivematerial under the well or wells of interest can pull assay 1000 intothe appropriate wells.

In some embodiments, microplate 20 can be made, at least in part, ofnon-electrically conductive materials. In some embodiments,non-electrically conductive materials can at least in part comprise oneor more of crystalline silica (3.0 W/mK), aluminum oxide (42 W/mK),diamond (2000 W/mK), aluminum nitride (150-220 W/mK), crystalline boronnitride (1300 W/mK), and silicon carbide (85 W/mK).

Microplate Surface Treatments

In some embodiments, the surface of the microplate 20 comprises anenhanced surface which can comprise a physical or chemical modality onor in the surface of the microplate so as to enhance support of, orfilling of, assay 1000 in a material retention region (e.g., a well or areaction spot). Such modifications can include chemical treatment of thesurface, or coating the surface. In some embodiments, such chemicaltreatment can comprise chemical treatment or modification of the surfaceof the microplate so as to form relatively hydrophilic and hydrophobicareas. In some embodiments, a surface tension array can be formedcomprising a pattern of hydrophilic sites forming material retentionregions on an otherwise hydrophobic surface, such that the hydrophilicsites can be spatially segregated by hydrophobic areas. Reagentsdelivered to the surface tension array can be retained by surfacetension difference between the hydrophilic sites and the hydrophobicareas.

In some embodiments, hydrophobic areas can be formed on the surface ofmicroplate 20 by coating microplate 20 with a photoresist substance andusing a photomask to define a pattern of material retention regions onmicroplate 20. After exposure of the photomasked pattern, at least aportion of the surface of microplate 20 can be reacted with a suitablereagent to form a stable hydrophobic surface. Such reagents cancomprise, for example, one or more members of alkyl groups, such as, forexample, fluoroalkylsilane or long chain alkylsilane (e.g.octadecylsilane). The remaining photoresist substance can then beremoved and the solid support reacted with a suitable reagent, such asaminoalkyl silane or hydroxyalkyl silane, to form hydrophilic sites. Insome embodiments, microplate 20 can be first reacted with a suitablederivatizing reagent to form a hydrophobic surface. Such reagents cancomprise, for example, vapor or liquid treatment of fluoroalkylsiloxaneor alkylsilane. The hydrophobic surface can then be coated with aphotoresist substance, photopatterned, and developed.

In some embodiments, the exposed hydrophobic surface can be reacted withsuitable derivatizing reagents to form hydrophilic sites. For example,in some embodiments, the exposed hydrophobic surface can be removed bywet or dry etch such as, for example, oxygen plasma and then derivatizedby aminoalkylsilane or hydroxylalkylsilane treatment. The photoresistcoat can then be removed to expose the underlying hydrophobic areas.

The exposed surface can be reacted with suitable derivatizing reagentsto form hydrophobic areas. In some embodiments, the hydrophobic areascan be formed by fluoroalkylsiloxane or alkylsilane treatment. Thephotoresist coat can be removed to expose the underlying hydrophilicsites. In some embodiments, fluoroalkylsilane or alkylsilane can beemployed to form a hydrophobic surface. In some embodiments, aminoalkylsilane or hydroxyalkyl silane can be used to form hydrophilic sites. Insome embodiments, derivatizing reagents can comprise hydroxyalkylsiloxanes, such as allyl trichlorochlorosilane, and 7-oct-l-enyltrichlorochlorosilane; diol(bis-hydroxyalkyl)siloxanes; glycidyltrimethoxysilanes; aminoalkyl siloxanes, such as 3-aminopropyltrimethoxysilane; Dimeric secondary aminoalkyl siloxanes, such asbis(3-trimethoxysilylpropyl)amine; and combinations thereof.

In some embodiments, the surface of microplate 20 can be first reactedwith a suitable derivatizing reagent to form hydrophilic sites. Suitablereagents can comprise, for example, vapor or liquid treatment ofaminoalkylsilane or hydroxylalkylsilane. The derivatized surface canthen be coated with a photoresist substance, photopatterned, anddeveloped. In some embodiments, hydrophilic sites can be formed on thesurface of microplate 20 by forming the surface, or chemically treatingit, with compounds comprising free amino, hydroxyl, carboxyl, thiol,amido, halo, or sulfate groups. In some embodiments, the free amino,hydroxyl, carboxyl, thiol, amido, halo, or sulfate group of thehydrophilic sites can be covalently coupled with a linker moiety (e.g.,polylysine, hexethylene glycol, and polyethylene glycol).

In some embodiments, hydrophilic sites and hydrophobic areas can be madewithout the use of photoresist. In some embodiments, a substrate can befirst reacted with a reagent to form hydrophilic sites. At least somethe hydrophilic sites can be protected with a suitable protecting agent.The remaining, unprotected, hydrophilic sites can be reacted with areagent to form hydrophobic areas. The protected hydrophilic sites canthen be unprotected. In some embodiments, a glass surface can be reactedwith a reagent to generate free hydroxyl or amino sites. Thesehydrophilic sites can be reacted with a protected nucleoside couplingreagent or a linker to protect selected hydroxyl or amino sites. In someembodiments, nucleotide coupling reagents can comprise, for example, aDMT-protected nucleoside phosphoramidite, and DMT-protectedH-phosphonate. The unprotected hydroxyl or amino sites can be reactedwith a reagent, for example, perfluoroalkanoyl halide, to formhydrophobic areas. The protected hydrophilic sites can then beunprotected.

In some embodiments, the chemical modality can comprise chemicaltreatment or modification of the surface of microplate 20 so as toanchor one or more components of assay 1000 to the surface. In someembodiments, one or more components of assay 1000 can be anchored to thesurface so as to form a patterned immobilization reagent array ofmaterial retention regions. In some embodiments, the immobilizationreagent array can comprise a hydrogel affixed to microplate 20. In someembodiments, hydrogels can comprise cellulose gels, such as agarose andderivatized agarose; xanthan gels; synthetic hydrophilic polymers, suchas cross-linked polyethylene glycol, polydimethyl acrylamide,polyacrylamide, polyacrylic acid (e.g., cross-linked with dysfunctionalmonomers or radiation cross-linking), and micellar networks; andmixtures thereof. In some embodiments, derivatized agarose can compriseagarose which has been chemically modified to alter its chemical orphysical properties. In some embodiments, derivatized agarose cancomprise low melting agarose, monoclonal anti-biotin agarose,streptavidin derivatized agarose, or any combination thereof.

In some embodiments, an anchor can be an attachment of a reagent to thesurface, directly or indirectly, so that one or more reagents isavailable for reaction during a chemical or amplification method, but isnot removed or otherwise displaced from the surface prior to reactionduring routine handling of the substrate and sample preparation prior touse. In some embodiments, assay 1000 can be anchored by covalent ornon-covalent bonding directly to the surface of the substrate. In someembodiments, assay 1000 can be bonded, anchored, or tethered to a secondmoiety (immobilization moiety) which, in turn, can be anchored to thesurface of microplate 20. In some embodiments, assay 1000 can beanchored to the surface through a chemically releasable or cleavablesite, for example by bonding to an immobilization moiety with areleasable site. Assay 1000 can be released from microplate 20 uponreacting with cleaving reagents prior to, during, or after manufacturingof microplate 20. Such release methods can include a variety ofenzymatic, or non-enzymatic means, such as chemical, thermal, orphotolytic treatment.

In some embodiments, assay 1000 can comprise a primer, which isreleasable from the surface of microplate 20. In some embodiments, aprimer can be initially hybridized to a polynucleotide immobilizationmoiety, and subsequently released by strand separation from thearray-immobilized polynucleotides during manufacturing of microplate 20.In some embodiments, a primer can be covalently immobilized onmicroplate 20 via a cleavable site and released before, during, or aftermanufacturing of microplate 20. For example, an immobilization moietycan contain a cleavable site and a primer. The primer can be releasedvia selective cleavage of the cleavable sites before, during, or afterassembly. In some embodiments, the immobilization moiety can be apolynucleotide which contains one or more cleavable sites and one ormore primer polynucleotides. A cleavable site can be introduced in animmobilized moiety during in situ synthesis. Alternatively, theimmobilized moieties containing releasable sites can be prepared beforethey are covalently or noncovalently immobilized on the solid support.In some embodiments, chemical moieties for immobilization attachment tosolid support can comprise carbamate, ester, amide, thiolester,(N)-functionalized thiourea, functionalized maleimide, amino, disulfide,amide, hydrazone, streptavidin, avidin/biotin, and gold-sulfide groups.

In some embodiments, microplate 20 can be coated with one or more thinconformal isotropic coatings operable to improve the surfacecharacteristics of the microplate, the material retention regions, orboth, for conducting a chemical or amplification reaction. In someembodiments, such treatments improve wettability of the surface, lowmoisture transmissivity of the surface, and high service temperaturecharacteristics of the substrate.

Microplate Molding

In some embodiments, microplate 20 can be molded by first extruding amelt blend comprising a mixture of a polymer and one or more thermallyconductive materials and/or additives. In some embodiments, the polymerand thermally conductive additives can be fed into a twin-screw extruderusing a gravimetric feeder to create a well-dispersed melt blend. Insome embodiments, the extruded melt blend can be transferred through awater bath to cool the melt blend before being pelletized and dried. Thepelletized melt blend can then be heated above its melting point by aninjection molding machine and then injected into a mold cavity. The moldcavity can generally conform to a desired shape of microplate 20. Insome embodiments, the injection-molding machine can cool the injectedmelt blend to create microplate 20. Finally, microplate 20 can beremoved from the injection-molding machine.

In some embodiments, two or more material types of pellets can be mixedtogether and the combination then placed in the injection moldingmachine to be melt blended during the injection molding process. In someembodiments, microplate 20 can be molded by first receiving pelletmaterial from a resin supplier; drying the pellet material in a resindryer; transferring the dried pellet material with a vacuum system intoa hopper of a mold press; molding microplate 20; trimming any resultantgates or flash; and packaging microplate 20. In some embodiments, themold cavity can be centrally gated along the second surface 24 ofmicroplate 20. In some embodiments, the mold cavity can be gated along aperimeter of main body 28 and/or skirt portion 30 of microplate 20.

Microplate Filling

In some embodiments, one or more devices or fluid interconnect systemscan be used to facilitate the placement of one or more components ofassay 1000 within at least some of the plurality of wells 26 ofmicroplate 20.

In some embodiments, microplate 20 can additionally comprise a fillingfeature, which is operable to facilitate filling of reagents and/orsamples into the material retention regions of microplate. In someembodiments, filling devices can include, for example, physical andchemical modalities that direct, channel, route, or otherwise effectflow of reagents or samples on the surface of microplate 20, on thesurface of sealing cover 80, or combinations thereof. In someembodiments, the filling device effects flow of reagents into materialretention regions. In some embodiments, microplate 20 can compriseraised or depressed regions (e.g., barriers and trenches) to aid in thedistribution and flow of liquids on the surface of the microplate. Insome embodiments, the filling system comprises capillary channels. Thedimensions of these features are variable, depending on factors, such asavoidance of air bubbles during use, handling convenience, andmanufacturing feasibility.

In some embodiments, a filling apparatus 400 can be used to fill atleast some of the plurality of wells 26 of microplate 20 with one ormore components of assay 1000. It should be understood that fillingapparatus 400 can comprise any one of a number of configurations.

In some embodiments, referring to FIGS. 20-22( b), filling apparatus 400comprises one or more assay input ports 402, such as about 96 inputports, disposed in an input layer 404. In some embodiments, assay inputports 402 of input layer 404 can be in fluid communication with aplurality of microfluidic channels 406 disposed in input layer 404, anoutput layer 408, or any other layer of filling apparatus 400. In someembodiments, the plurality of microfluidic channels 406 can be formed inan underside of input layer 404 and a seal member can be placed over theunderside of input layer 404. In some embodiments, the seal member cancomprise a perforation (e.g. hole) positioned over a desired location inmicroplate 20 to permit a discrete fluid communication passage to extendtherethrough. In some embodiments, the plurality of microfluidicchannels 406 can be arranged as a grouping 407 (FIG. 20). In someembodiments, assay input ports 402 can be positioned at a predeterminedpitch (e.g. 9 mm) such that each assay input port 402 can be alignedwith a center of each grouping 407. In some embodiments, the pluralityof microfluidic channels 406 can be in fluid communication with aplurality of staging capillaries 410 formed in output layer 408 (FIGS.21-22( b)).

In some embodiments, input layer 404 and output layer 408 can be bondedor otherwise joined together to form a single unit. This bond can bemade with, among other things, a double-stick tape, a laser weld, anultrasonic weld, or an adhesive. However, it should be appreciated thatthe bonding or otherwise joining of input layer 404 and output layer 408is not required.

During filling, assay 1000 can be put into at least one assay input port402 and can be fluidly channeled toward at least one of the plurality ofmicrofluidic channels 406, first passing a surface tension relief post418 in some embodiments. In some embodiments, surface tension reliefpost 418 can serve, at least in part, to evenly spread assay 1000throughout the plurality of microfluidic channels 406 and/or engage ameniscus of assay 1000 to encourage fluid flow. Assay 1000 can befluidly channeled through the plurality of microfluidic channels 406 andcan collect in the plurality of staging capillaries 410 (FIG. 22( b)).Assay 1000 can then be held in the plurality of staging capillaries 410by capillary or surface tension forces.

In some embodiments, as illustrated in FIGS. 21 and 22( a)-(b),microplate 20 can be attached to filling apparatus 400 so that each ofthe plurality of staging capillaries 410 is generally aligned with eachof the plurality of wells 26. In some embodiments, filling apparatus 400comprises alignment features 411 (FIG. 20) operably sized to engagecorresponding alignment feature 58 on microplate 20 to, at least inpart, facilitate proper alignment of each of the plurality of stagingcapillaries 410 with a corresponding (respective) one of the pluralityof wells 26. In some embodiments, the combined unit of filling apparatus400 and microplate 20 can then be placed in a centrifuge. Thecentrifugal force of the centrifuge can, at least in part, urge assay1000 from the plurality of staging capillaries 410 into each of theplurality of wells 26 of microplate 20. Filling apparatus 400 can thenbe removed from microplate 20. In some embodiments, microplate 20 canthen receive additional reagents and/or be sealed with sealing cover 80,or other sealing feature such as a layer of mineral oil, and then placedinto high-density sequence detection system 10.

In some embodiments, capillary or surface tension forces encourage flowof assay 1000 through staging capillaries 410. In this regard, stagingcapillaries 410 can be of capillary size, for example, stagingcapillaries 410 can be formed with an exit diameter less than about 500micron, and in some embodiments less than about 250 microns. In someembodiments, staging capillaries 410 can be formed, for example, with adraft angle of about 1-5° and can define any thickness sufficient toachieve a predetermined volume. To further encourage the desiredcapillary action in staging capillaries 410, staging capillaries 410 canbe provided with an interior surface that is hydrophilic, i.e.,wettable. For example, the interior surface of staging capillaries 410can be formed of a hydrophilic material and/or treated to exhibithydrophilic characteristics. In some embodiments, the interior surfacecomprises native, bound, or covalently attached charged groups. Forexample, one suitable surface, according to some embodiments, is a glasssurface having an absorbed layer of a polycationic polymer, such aspoly-l-lysine.

Ramps

In some embodiments, as illustrated in FIGS. 22( b) and 23(a)-(b), eachof the plurality of staging capillaries 410 can comprise a ramp feature414 disposed at an entrance thereof to achieve a predetermined capillaryaction. It should be appreciated that ramp feature 414 can be formed onone or more edges of the entrance to each of the plurality of stagingcapillaries 410. In some embodiments, ramp feature 414 can comprise acountersink lip or chamfered rim formed about the entire entrance. Insome embodiments that do not employ the plurality of microfluidicchannels 406, ramp feature 414 can be used to reduce an angle betweenstaging capillary 410 and an upper surface 456 (to be described herein)of output layer 408 to aid in capillary flow and/or exposure time to afluid bead moving thereby.

Nozzles Bottom Features

In some embodiments, with reference to FIGS. 22( b) and 24, output layer408 can comprise a protrusion 450 formed on an outlet 434 of stagingcapillary 410. In some embodiments, protrusion 450 can be shaped tocooperate with a corresponding shape of each of the plurality of wells26. In some embodiments, protrusion 450 can be conically shaped to bereceived within circular rim portion 32 of each of the plurality ofwells 26. In some embodiments, protrusion 450 can be square-shaped to bereceived within square-shaped rim portion 38 of each of the plurality ofwells 26. Protrusion 450, in some embodiments, can define a sufficientlysharp surface such that the capillary force within staging capillary 410can retain assay 1000 and protrusion 450 can inhibit movement of assay1000 to adjacent wells 26. In some embodiments, protrusion 450 of outputlayer 408 can be positioned above microplate 20, flush with firstsurface 22 of microplate 20 (FIG. 22( a)), or disposed within well 26 ofmicroplate 20 (FIG. 22( b)). In some embodiments, protrusion 450 candefine a nozzle feature that comprises a diameter that is less than thediameter of the plurality of wells 26 to aid, at least in part, incapillary retention of assay 1000 within staging capillary 410.

Protrusion 450 can be provided with an exterior surface that ishydrophobic, i.e., one that causes aqueous medium deposited on thesurface to bead. For example, protrusion 450 can be formed of ahydrophobic material and/or treated to exhibit hydrophobiccharacteristics. This can be useful, for example, to prevent spreadingof a drop, formed at tip portion 1840. A variety of known hydrophobicpolymers, such as polystyrene, polypropylene, and/or polyethylene, canbe utilized to obtain desired hydrophobic properties. In addition, or asan alternative, a variety of lubricants or other conventionalhydrophobic films can be applied to tip portion 1840.

Bottom Feature—Spacer

In some embodiments, as illustrated in FIG. 24, one or more spacermembers 452 can be formed along bottom surface 429 of output layer 408to, at least in part, achieve a desired spacing between output layer 408and microplate 20. In some embodiments, spacer member 452 can be formedas an elongated member (FIG. 24), a post (FIG. 35), one or morespaced-apart members, or the like.

Fluidic Patterns

In some embodiments, as illustrated in FIGS. 23( a)-(b) and 25(a)(f),the plurality of microfluidic channels 406 can have any one of aplurality of configurations for carrying assay 1000 to each of theplurality of staging capillaries 410. In some embodiments, each of theplurality of staging capillaries 410 can be in fluid communication withonly one of the plurality of microfluidic channels 406 (FIGS. 23(a)-(b), 25(a)-(d), and 25(f)) in a series-type configuration. In someembodiments, each of the plurality of staging capillaries 410 can be influid communication with two or more of the plurality of microfluidicchannels 406 (FIG. 25( e)) in a multi-path or parallel-typeconfiguration. In such parallel-type configurations, fluid can flowalong the path of least resistance to fill each of the plurality ofstaging capillaries 410 in the least amount of time. In anyconfiguration, the time required to fill each of the plurality ofstaging capillaries 410 can be reduced by reducing the length of eachmicrofluidic channel 406. In some embodiments, a hybrid of theseries-type and the parallel-type configurations can be used. In someembodiments, as illustrated in FIG. 25( f), each of the plurality ofmicrofluidic channels 406 can be in fluid communication with only oneedge of each of the plurality of staging capillaries 410 to providepass-by and filling action simultaneously.

In some embodiments, each of the plurality of microfluidic channels 406can exert, at least in part, a capillary force to draw fluid (e.g. assay1000) therein to aid in reducing the time required to fill. Thecapillary force of each of the plurality of microfluidic channels 406can be varied, at least in part, by varying at least the dimensionalproperties of the plurality of microfluidic channels 406 according tocapillary principles.

Pressure Nodules

In some embodiments, as illustrated in FIGS. 33-40, filling apparatus400 comprises input layer 404, output layer 408, and an intermediatelayer 494, or any combination thereof for filling one or more componentsof assay 1000 into at least some of the plurality of wells 26 inmicroplate 20.

In some embodiments, intermediate layer 494 can be positioned andaligned between input layer 404 and output layer 408. In someembodiments, input layer 404 comprises assay input ports 402 extendingtherethrough. As illustrated in FIGS. 34 and 35, in some embodiments,each assay input port 402 can extend through input layer 404 andterminate at an extended outlet 496. In some embodiments, extendedoutlet 496 can be sized to extend from input layer 404 such that an end498 of extended outlet 496 is spaced a predetermined distance fromoutput layer 408 (FIG. 34). Extended outlet 496 can extend through acorresponding aperture 500 (FIG. 33) formed through intermediate layer494.

In some embodiments, as illustrated in FIG. 34, extended outlet 496 canbe aligned with surface tension relief post 418 extending upward fromoutput layer 408. In some embodiments, an internal diameter of extendedoutlet 496 can be larger than an outer diameter of surface tensionrelief post 418 to permit surface tension relief post 418 to be at leastpartially received within extended outlet 496. Surface tension reliefpost 418, in some embodiments, can be sufficiently sized to facilitateeven spreading of assay 1000 throughout the plurality of microfluidicchannels 406 and/or engage a meniscus of assay 1000 within assay inputport 402 to encourage flow. In some embodiments, extended outlet 496 andsurface tension relief post 418 can cooperate to facilitate alignmentsof input layer 404, output layer 408, and intermediate layer 494.

In some embodiments, intermediate member 494 comprises microfluidicchannels 406 extending there along (e.g., etched or otherwise formed inone major side thereof) in fluid communication with the plurality ofstaging capillaries 410 in output layer 408. For example, microfluidicchannels 406, extending along a lower surface of intermediate layer 494,can communicate with upper-end openings of staging capillaries 410. Itshould be appreciated that the particular route configuration ofmicrofluidic channels 406 can be any one of a number of configurationsselected by one skilled in the art or one of those described herein. Insome embodiments, intermediate member 494 can be compliant, orresiliently deformable, to permit flexing of intermediate member 494 inresponse to an external force. In some embodiments, intermediate member494 can be made of polymeric materials, such as but not limited torubber or silicone (PDMS).

As illustrated in FIGS. 35-38, in some embodiments, input layer 404comprises one or more nodules 502 extending from a bottom surface 504.In some embodiments, nodules 502 can be patterned along bottom surface504 such that each nodule 502 can engage a top surface 506 of compliantintermediate layer 494. During centrifugation, centripetal force exertedon input layer 404 can cause nodules 502 to engage compliantintermediate layer 494 to at least partially collapse or depress asegment of intermediate layer 494 against output layer 408 to minimizefluid communication between adjacent staging capillaries 410. In someembodiments, as illustrated in FIGS. 36 and 37, nodules 502 can bepatterned such that each nodule 502 is positioned adjacent each of theplurality of staging capillaries 410. For example, nodules 502 can bedisposed so that each nodule aligns, or corresponds, with a respectiveone of staging capillaries 410. In some embodiments, nodules 502 can bepatterned over portions of microfluidic channels 406 to closemicrofluidic channel 406 during centrifugation. In some embodiments, asillustrated in FIG. 38, nodules 502 can be patterned over each of theplurality of staging capillaries 410 to seal each of the plurality ofstaging capillaries 410 during centrifugation. For example, upon beingdepressed by nodules 502 during centrifugation, segments of intermediatelayer 494 can seal the upper end openings of respective, correspondingstaging capillaries 410.

In some embodiments, as illustrated in FIGS. 38 and 39, a sealingfeature 508 can extend from intermediate layer 494 that can be sized tofit into the corresponding staging capillary 410 by nodule 502 actingupon intermediate layer 494. These, and substantially equivalent,embodiments can be used to define a shut-off valve during centrifugationor anytime a force is applied to input layer 404 and/or intermediatelayer 494.

It should be appreciated that the physical size and/or compliancy of oneof more of input layer 404, intermediate layer 494, nodules 502, andsealing features 508 can be tailored to achieve a predetermined sealingengagement upon application of a predetermined amount of force.Additionally, it should be appreciated that nodules 502 and/or sealingfeature 508 can be of any shape conducive to applying a force andsealing an opening, respectively, such as, but not limited to,triangular, square, or conical.

In some embodiments, to load each of the plurality of stagingcapillaries 410, a predetermined amount of assay 1000 can be placed ateach assay input port 402. Capillary force, at least in part, can drawat least a portion of assay 1000 from assay input port 402 intomicrofluidic channels 406 and further fill at least some of theplurality of staging capillaries 410. In some embodiments, once at leastsome of the plurality of staging capillaries 410 are filled, outputlayer 408 and microplate 20 can be placed into a swing-arm centrifuge.In some embodiments, the centripetal force of the swing-arm centrifugecan be sufficient to overcome the surface tension of assay 1000 in eachthe plurality of staging capillaries 410, thereby forcing a meteredvolume of assay 1000 into each of the plurality of wells 26 ofmicroplate 20. In some embodiments, the centripetal force of thecentrifuge can be sufficient to exert a clamping force on at least oneof input layer 404 and intermediate layer 494 to fluidly seal adjacentstaging capillaries 410, either at the entrance thereof or therebetween,to prevent residual assay 1000 left in assay input port 402 or assay1000 from an undesired one of the plurality of wells 26 of microplate 20from overfilling a particular staging capillary. In some embodiments, anexternal force (e.g. mechanical, pneumatic, hydraulic,electro-mechanical, and the like) can be applied to exert a clampingforce on at least one of input layer 404 and intermediate layer 494 tofluidly seal adjacent staging capillaries 410, either at the entrancethereof or therebetween.

In some embodiments, as illustrated in FIG. 40, at least some of inputlayer 404, intermediate layer 494, and output layer 408 can be used inconjunction with a clamp system 511. In some embodiments, clamp system511 comprises a base structure 513 and one or more locking features 515extending therefrom. In some embodiments, base structure 513 comprisesat least one alignment feature 517 operably sized to engage acorresponding alignment feature 58 on microplate 20 to, at least inpart, facilitate proper alignment of each of the plurality of stagingcapillaries 410 relative to each of the plurality of wells 26. In someembodiments, alignment feature 517 can further engage a correspondingalignment feature 519 formed in at least one of input layer 404,intermediate layer 494, and output layer 408. In some embodiments, atleast some of microplate 20, input layer 404, intermediate layer 494,and output layer 408 can be coupled with base structure 513 such thatlocking feature 515 engages input layer 404 to exert a preload onintermediate layer 494 to prevent fluid flow and/or leakage of assay1000 prior to achieving sufficient centrifugal speed in the centrifuge.In some embodiments, a top plate 521 can be used in conjunction withbase structure 513 to ensure equal pressure application across inputlayer 404 by locking feature 515.

Venting

In some embodiments, as illustrated in FIGS. 41-46, filling apparatus400 comprises input layer 404, output layer 408, and a vent layer 523,or any combination thereof for loading assay 1000 into at least some ofthe plurality of wells 26 in microplate 20. In some embodiments, outputlayer 408 comprises microfluidic channels 406 formed in a side thereofand extending there along in fluid communication with the plurality ofstaging capillaries 410 in output layer 408.

In some embodiments, input layer 404 comprises assay input ports 402extending therethrough. As illustrated in FIGS. 42-43, in someembodiments, each assay input port 402 can extend through input layer404 and terminate at extended outlet 496. In some embodiments, extendedoutlet 496 can be sized to extend from input layer 404 such that an end498 of extended outlet 496 is generally flush to a top surface 525 ofvent layer 523 and aligned to a flow aperture 527 extending through ventlayer 523.

In some embodiments, input layer 404 comprises one or more vent features529 (FIGS. 43-46). In some embodiments, vent feature 529 can be sized tohave a capillary force associated therewith that is lower than acapillary force within microfluidic channels 406 and/or each of theplurality of staging capillaries 410 to reduce the likelihood of assay1000 flow through or into vent feature 529. In some embodiments, ventfeature 529 comprises a vent hole 531 extending through input layer 404(FIGS. 41-45) and in communication with atmosphere. In some embodiments,vent hole 531 can be coupled to a chamber or manifold 533 (FIGS. 42 and43) that can couple two or more vent apertures 535 formed in vent layer523 to atmosphere.

In some embodiments, vent feature 529 comprises a pressure bore 537(FIG. 44) associated with one or more of the plurality of stagingcapillaries 410. In some embodiments, pressure bore 537 can be formed ininput layer 404. For example, pressure bore 537 can extend from a lowersurface of input layer 404 toward, but stopping short of, an opposingsurface. In some embodiments, plural pressure bores 537 are disposed inan array corresponding to an array defined by staging capillaries 410.Pressure bores 537, in some embodiments, can be sized to act as an aircapacitor trapping a portion of air therein that can contract or expandduring filling of assay 1000 into filling apparatus 400 and/orcentrifuging assay 1000 into each of the plurality of wells 26,respectively.

Vent feature 529, in some embodiments, can at least partially relievevacuum created when assay 1000 is centrifuged from each of the pluralityof staging capillaries 410 into each of the corresponding plurality ofwells 26 of microplate 20 and permit improved loading. In someembodiments, vent feature 529 can at least partially interrupt fluidflow between adjacent staging capillaries 410 by introducing an air gaptherebetween. In some embodiments, such an air gap can provideconsistent metering of assay 1000 loaded into each of the plurality ofwells 26.

In some embodiments, vent layer 523 can be positioned and alignedbetween input layer 404 and output layer 408. In some embodiments, asillustrated in FIG. 43, flow aperture 527 of vent layer 523 can bealigned with surface tension relief post 418 extending upward fromoutput layer 408. In some embodiments, an internal diameter of flowaperture 527 can be larger than the outer diameter of surface tensionrelief post 418 to permit surface tension relief post 418 to be at leastpartially received within flow aperture 527. Surface tension relief post418, in some embodiments, can be sufficiently sized to facilitate evenspreading of assay 1000 throughout the plurality of microfluidicchannels 406 in output layer 408 and/or engage a meniscus of assay 1000within assay input port 402 and/or flow aperture 527 to encourage flow.In some embodiments, extended outlet 496, flow aperture 527, and surfacetension relief post 418 can cooperate to facilitate alignments of inputlayer 404, output layer 408, and vent layer 523.

As illustrated in FIGS. 43-45, in some embodiments, vent layer 523 canbe aligned with input layer 404 and output layer 408 such that ventapertures 535 are positioned above or between each of the plurality ofstaging capillaries 410. In some embodiments, vent apertures 535 can bea circular bore (FIG. 44) or any other shape, such as oblong (FIG. 45),to accommodate for potential misalignment between input layer 404 andvent layer 523 and/or potential misalignment between vent layer 523 andoutput layer 408.

In some embodiments, vent layer 523 can be made of any materialconducive to joining with input layer 404 and/or output layer 408. Insome embodiments, vent layer 523 can comprise PDMS, which can aid injoining vent layer 523 to input layer 404 due to the intrinsic tackinessproperties of PDMS. In some embodiments, vent layer 523 can be madeusing a double stick adhesive tape. In such embodiments, the doublestick adhesive tape can be first applied to input layer 404 and thenlaser cut to accurately place vent apertures 535 to simplify assembly ofinput layer 404 and vent layer 523.

In some embodiments, to load each of the plurality of stagingcapillaries 410, a predetermined amount of assay 1000 can be placed ateach assay input port 402. Such placement can be effected, for example,using an automated pipette system (e.g., a Biomek) or hand-operatedsingle- or multi-channel pipette device (e.g., a Pipetman). Capillaryforce, at least in part, can draw at least a portion of assay 1000 fromassay input port 402 into microfluidic channels 406 and further fill atleast some of the plurality of staging capillaries 410. In someembodiments, outlet 434 of each of the plurality of staging capillaries410 permits venting of air within each of the plurality of stagingcapillaries 410 during filling. In some embodiments, once at least someof the plurality of staging capillaries 410 are filled, input layer 404,vent layer 523, output layer 408, and microplate 20 can be placed into aswing-arm centrifuge. In some embodiments, the venting features 529 canreduce vacuum effects on assay 1000 during centrifugation to more easilymeter a volume of assay 1000 into each of the plurality of wells 26 ofmicroplate 20.

Capillary Plane

In some embodiments, as illustrated in FIGS. 108-119, filling apparatus400 comprises input layer 404 and output layer 408 for loading assay1000 (see FIG. 110) into at least some of the plurality of wells 26 inmicroplate 20. Input layer 404 comprises, in some embodiments, one ormore assay input ports 402 each in fluid communication with at least aportion of the plurality of microfluidic channels 406 disposed in outputlayer 408. Assay input ports 402 can be configured to receive assay 1000from any one of a number of sources, such as a pipette (see FIG. 110).

As illustrated in FIGS. 108-109, assay input ports 402 can comprise ageometry having a generally X-shaped depression; a central,upwardly-shaped member 1900; and radially extending arm channels 1902terminating at through-holes 1904. In this regard, assay 1000 can besplit to the four through-holes 1904 by virtue of fluid flow for quickand even filling.

Central, upwardly-shaped member 1900 can define any cross-sectionalshape that is conducive to a particular application. In someembodiments, as illustrated in FIGS. 110-119, central, upwardly-shapedmember 1900 can comprise a centrally-raised portion 1906 havingdownwardly-sloping sides 1908. Downwardly-sloping sides 1908 can be acontinuous surface sweeping about centrally-raised portion 1906 or canbe distinct surfaces descending from centrally-raised portion 1904,thereby providing flow direction control. In some embodiments, central,upwardly-shaped member 1900 can comprise a generally smooth contouredshape conducive to distributing assay 1000 with minimum splash back.Furthermore, central, upwardly-shaped member 1900 can serve to minimizepenetration of pipette tip (see FIG. 110) within the structure of theplurality of microfluidic channels 406 disposed in output layer 408 byphysically preventing its insertion. Additionally, central,upwardly-shaped member 1900 can serve to minimize the force of fluidflow of assay 1000, thereby minimizing the chance of overcoming thesurface tension and/or capillary force of assay 1000 contained in theplurality of staging capillaries 410.

In some embodiments, output layer 408 comprises a microfluidic structure1910 in fluid communication with the plurality of staging capillaries410 for quickly distributing assay 1000 to the plurality of stagingcapillaries 410. In some embodiments, microfluidic structure 1910comprises the plurality of microfluidic channels 406, arranged in adesired pattern or routing structure upon output layer 408, and acapillary plane 1912. More particularly, the plurality of microfluidicchannels 406 can be arranged such that they fluidly interconnect two ormore adjacent staging capillaries 410. Each of the plurality ofmicrofluidic channels 406 can have a width and depth that is selected toachieve a desired capillary force. In some embodiments, the plurality ofmicrofluidic channels 406 can be arranged as a grouping 407 (FIG. 108).In some embodiments, assay input ports 402 can be positioned at apredetermined pitch (e.g. 9 mm) such that a central axis of each assayinput port 402 can be aligned with a center or other predeterminedlocation of each grouping 407. Additionally, as discussed herein, atleast some of the plurality of microfluidic channels 406 can compriseramp features, surface treatments, and/or other features to achievedesired filling characteristics. These characteristics may varydepending on the size of staging capillaries 410, the type of assay1000, the necessary fill times, and the like.

As illustrated in FIGS. 120-112 and 128-135, the plurality ofmicrofluidic channels 406 can be arranged in any one of a number oforientations. For example, in some embodiments, the plurality ofmicrofluidic channels 406 can be arranged in a cross-pattern (see FIGS.120-121) to provide multiple fluid paths for assay 1000 to flow. In thiscross-pattern, each of the plurality of staging capillaries 410 canreceive assay 1000 by two or more microfluidic channels 406 to reducefill time. While, in some embodiments, the plurality of microfluidicchannels 406 can be arranged in an S-shape pattern as illustrated inFIG. 122. In this regard, each of the plurality of microfluidic channels406 and the plurality of staging capillaries 410 are filled in seriesone after another. Referring to FIGS. 122-126, it should be noted thatthe illustrated S-shape pattern provides geometric restraint of assay1000 during centrifuge. That is, in some embodiments as illustrated inFIG. 122, there are no more than two staging capillaries 410 coupledtogether via microfluidic channels 406 in the X-direction. Therefore,during the initial centrifuging of assay 1000 into each of the pluralityof wells 26 of microplate 20, assay 1000 is inhibited from movement todownstream staging capillaries 410 in the X-direction. If the S-shapedpattern was shifted by 90 degrees, during centrifuge assay 1000 could beinitially forced to one end of grouping 407 and could overfillassociated wells 26 of microplate 20.

Additionally, in some embodiments as illustrated FIGS. 128-130, theplurality of microfluidic channels 406 can be arranged in a diagonalpattern relative the X-direction and the Y-direction. This arrangementprovides microfluidic channels that do not reside in either theX-direction or Y-direction but rather at an angle thereto. In someembodiments, the plurality of microfluidic channels 406 can be generallydisposed at an angle of about 15 degrees to about 90 degrees relative tothe X-direction (i.e. the direction of the applied centripetal forceduring early centrifugation).

In some embodiments, as illustrated in FIGS. 131-132, the plurality ofmicrofluidic channels 406 can be arranged in an H-shaped pattern. Inthis arrangement, adjacent staging capillaries 410 are fluidly coupledin series via microfluidic channels 406 along a fluidic row 1924 in theY-direction (see FIG. 132). In some embodiments, each fluidic row 1924can be interconnected to an adjacent fluidic row 1924 via a fluidicconnector 1926 in the X-direction. In this arrangement, assay 1000 canfreely flow along fluidic rows 1924 (Y-direction) to fill the pluralityof staging capillaries 410 and further flow to adjacent fluidic rows1924 along fluidic connectors 1926 (X-direction). However, duringcentrifugation, angular acceleration, which will be substantiallyapplied in the X-direction, will not cause a substantial amount of assay1000 to flow to downstream staging capillaries 410. To further minimizethis flow, fluidic connectors 1926 can be arranged such that they areoffset relative to each other in the Y-direction as illustrated in FIG.132. This minimizes the length of any fluidic channel extending in theX-direction.

In some embodiments, as illustrated in FIGS. 133-135, the plurality ofmicrofluidic channels 406 can comprise two or more S-shaped fluidicpatterns 1928 interconnected by a plurality of fluidic connectors 1926disposed in a Y-direction (see FIG. 134). Specifically, in someembodiments, S-shaped fluidic patterns 1928 can comprise a plurality offirst fluidic portions 1930 extending in a Y-direction fluidlyconnecting two or more staging capillaries 410. A plurality of secondfluidic portion 1932 extending in an X-direction can be fluidly coupledbetween the plurality of fluidic portions 1930 in an alternating patternto define S-shaped fluidic patterns 1928. Fluidic connectors 1926 canfluidly couple adjacent second fluidic portions 1932 in a Y-direction.This arrangement generally minimizes the number of staging capillaries410 connected in the Y-direction to provide additional resistance toundesirable flow of assay 1000.

In some embodiments, output layer 408 can comprise one or more surfacetension relief post 418 can be disposed in through-holes 1904 to, atleast in part, evenly spread assay 1000 throughout the plurality ofmicrofluidic channels 406 and/or engage a meniscus of assay 1000 toencourage fluid flow. Surface tension relief post 418 can, according tosome embodiments, be hydrophilic in order to further encourage fluidflow into through-holes 1904 and, thus, microfluidic channels 406. Insome embodiments, an internal diameter of through-holes 1904 can belarger than an outer diameter of surface tension relief post 418 topermit surface tension relief post 418 to be at least partially receivedwithin through-holes 1904. In some embodiments, through-holes 1904 andsurface tension relief posts 418 can cooperate to facilitate alignmentof input layer 404 and output layer 408.

In some embodiments, input layer 404 and output layer 408 can bephysically coupled together, using, for example, adhesive and/orchemical bonding, laser welding, and/or ultra-sonic welding, asillustrated in FIG. 109, to form a unitary member. In doing so, bottomsurface 504 of input layer 404 (see FIG. 110) can span a topside ofoutput layer 408. In some embodiments, bottom surface 504 of input layer404 can engage or otherwise sealingly contact a first surface 1914 ofoutput layer 408 to define an interface generally resistant to fluidflow. As input layer 404 and output layer 408 are brought together, asecond surface 1916 of output layer 408 is spaced apart from bottomsurface 504 of input layer 404 to form a volume. In other words, in someembodiments, second surface 1916 is lower than first surface 1914.Accordingly, this formed volume, bound by bottom surface 504, secondsurface 1916, and the interface between first surface 504 and bottomsurface 504 forms capillary plane 1912. In some embodiments, asillustrated in FIGS. 120-122, capillary plane 1912 can receive assay1000 therein and form a single, generally continuous, fluid sheet acrossgrouping 407. In this regard, during filling, assay 1000 would firstgenerally spread across capillary plane 1912 and then be rapidly andefficiently drawn into the plurality of microfluidic channels 406 andstaging capillaries 410. In some embodiments, all corners withincapillary plane 1912 are rounded to reduce localized surface tension tominimize retention of assay 1000 in corners of capillary plane 1912 andfurther concentrate the flow of assay 1000 over the plurality ofmicrofluidic channels 406 and the plurality of staging capillaries 410.

In some embodiments, as illustrated in FIGS. 123-126, output layer 408can comprise one or more wall restraints 1918 disposed between at leastsome of the plurality of microfluidic channels 406 and the plurality ofstaging capillaries 410. In some embodiments, wall restraints 1918extend upward and engage bottom surface 504 to define an interfacegenerally resistant to fluid flow. Wall restraints 1918 can bepositioned in any position that aids fluid flow and/or controlsdistribution of assay 1000. However, it should be understood thatcapillary plane 1912 remains substantially continuous. In someembodiments, wall restraints 1918 can be centrally located with fluidflow openings 1920 on opposing ends thereof (FIGS. 123-124). In someembodiments, wall restraints 1918 can extend to one side of capillaryplane 1912 to define an S-shaped capillary plane 1912 (FIGS. 125-126).In some embodiments, wall restraints 1918 induce a stronger capillaryforce in capillary plane 1912 and further reduce the overall volume ofcapillary plane 1912 leading to reduced waste of assay 1000. In someembodiments, wall restraints 1918 can be used to oppose any fluid forcesacting in the X-direction (see FIG. 122) during centrifugation.

The strength of the capillary force generated by capillary plane 1912 isgeometrically determined by the distance between second surface 1916 ofoutput layer 408 and bottom surface 504 of input layer 404. The Laplacepressure generated can be controlled according to the followingrelationship:

${\Delta\; P_{la}} = \frac{2\left( {h + w} \right)\left( {\gamma_{sa} - \gamma_{sl}} \right)}{wh}$wherein

-   -   γsa=Surface tension at the Solid-Air boundary    -   γsl=Surface tension at the Solid-Liquid boundary    -   w=Width of the capillary plane    -   h=Height of the capillary plane

In some embodiments, the combination of capillary plane 1912 and theplurality of microfluidic channels 406 serves to affectively draw assay1000 into the plurality of staging capillaries 410 at a rate faster thanwithout capillary plane 1912. In some embodiments, the capillary forcegenerated increases from capillary plane 1912 to the plurality ofmicrofluidic channels 406 to the plurality of staging capillaries 410,thereby serving to evenly draw and load assay 1000 into the plurality ofstaging capillaries 410.

In some embodiments, capillary plane 1912 further provides a uniformpressure above each of the plurality of staging capillaries 410 duringcentrifuge. In some embodiments, this uniform pressure is equivalent toatmospheric pressure. That is, once capillary plane 1912 is evacuated ofassay 1000 during the filling process, the open expanse of capillaryplane 1912 can serve as a vent system venting the area above each of theplurality of staging capillaries 410 to atmosphere or other appliedpressure (or vacuum). In some embodiments, this arrangement serves toeliminate or, at least, minimize the formation of internal micro-vacuumsin what would be otherwise a closed and connected fluidic network. Theseinternal vacuums can induce purging of assay 1000 from both adjacentstaging capillaries 410 and/or entire fluid networks thereby leading toundesirable overfilling/under filling and reduced accuracy. By includinga vent and providing a thin volume of atmospheric pressure above theplurality of staging capillaries 410 the internal vacuums can be quicklydissipated. In some embodiments, the plurality of microfluidic channels406 can serve a dual functionality, in that they can provide a completecircuit of fluid connection between the plurality of staging capillaries410 and further assist in equilibrating the volume of assay 1000 fromcapillary plane 1912 over grouping 407 for improved filling accuracy andprecision.

During filling of embodiments having an unobstructed capillary plane1912 (see FIGS. 120-122), assay 1000 is first injected into assay inputports 402 of input layer 404 (FIG. 110). Capillary forces and/orgravitational pressures urge assay 1000 into and evenly across capillaryplane 1912 (FIGS. 126-111). The stronger capillary force of theplurality of microfluidic channels 406 draws assay 1000 therein andfurther urges assay 1000 toward the plurality of staging capillaries410. The stronger capillary force of the plurality of stagingcapillaries 410 draws assay 1000 therein from the plurality ofmicrofluidic channels 406 (FIG. 113).

During filling of embodiments having restraint walls 1918 disposed incapillary plane 1912 (see FIGS. 123-126), assay 1000 is injected intoassay input ports 402 of input layer 404 (FIG. 114). Capillary forcesand/or gravitational pressures urge assay 1000 into a portion ofcapillary plane 1912 bound by restraint walls 1918 (FIGS. 115-116).Assay 1000 then flows through and/or around restraint walls 1918 to fillcapillary plane 1912. Simultaneously, the stronger capillary force ofthe plurality of microfluidic channels 406 draws assay 1000 therein andfurther urges assay 1000 toward the plurality of staging capillaries410. The stronger capillary force of the plurality of stagingcapillaries 410 draws assay 1000 therein from the plurality ofmicrofluidic channels 406 (FIG. 117-119).

As illustrated in FIGS. 136-137, once the plurality of stagingcapillaries 410 have been filled with assay 1000, filling apparatus 400and microplate 20 are centrifuged in a swing-arm style centrifuge, whichserves to overcome the surface tension and/or capillary force of assay1000 within the plurality of staging capillaries 410, to urge assay 1000from the plurality of staging capillaries 410 to the plurality of wells26 of microplate 20. Initially, as illustrated in FIG. 136, fillingapparatus 400 and microplate 20 are subjected to a centripetalacceleration and angular acceleration. However, at steady-state, filingapparatus 40 and microplate 20 are generally subjected to a centripetalforce (see FIG. 137).

Open Channel Microfluidic Network

In some embodiments, the plurality of microfluidic channels 406 can bearranged to neutralize, minimize, suppress, or otherwise manipulate thefluid forces exerted during early stages of centrifugation in aswing-arm system centrifuge. In other words, in some embodiments, fluidflow forces can be managed through the use of various features,geometries, and spatial orientation of the plurality of microfluidicchannels 406 to improve precision and accuracy of the dispensed volumesof assay 1000.

In some embodiments, as illustrated in FIGS. 138-139, filling apparatus400 comprises input layer 404 and output layer 408 for loading assay1000 (see FIG. 140) into at least some of the plurality of wells 26 inmicroplate 20. Input layer 404 comprises, in some embodiments, one ormore assay input ports 402 each in fluid communication with at least aportion of the plurality of microfluidic channels 406 disposed in outputlayer 408. In some embodiments, each of the plurality of microfluidicchannels 406 comprises a pair of sidewalls, a bottom, and an opened top.Therefore, flow control of the plurality of microfluidic channels 406can be controlled by the sizing of the sidewalls and bottom (also knownas the aspect ratio).

Assay input ports 402 can be configured to receive assay 1000 from anyone of a number of sources, such as a pipette (see FIG. 140). Asillustrated in FIGS. 138-139, assay input ports 402 can comprisegenerally sloped sides extending to a through-hole in fluidcommunication with the plurality of microfluidic channels 406. In someembodiments, input layer 404 can comprise a plurality of open slots 1922formed there through. The plurality of open slots 1922 can be positionedabove at least some of the plurality of microfluidic channels 406 toprovide generally uniform, zero-air-resistance to the plurality ofstaging capillaries 410. The plurality of open slots 1922 can bearranged to maximize the number of the plurality of microfluidicchannels 406 and the plurality of staging capillaries 410 exposeddirectly to atmosphere.

In some embodiments, output layer 408 comprises a microfluidic structure1910 in fluid communication with the plurality of staging capillaries410 for quickly distributing assay 1000 to the plurality of stagingcapillaries 410. In some embodiments, microfluidic structure 1910comprises the plurality of microfluidic channels 406, arranged in adesired pattern or routing structure upon output layer 408, and acapillary plane 1912. More particularly, the plurality of microfluidicchannels 406 can be arranged such that they fluidly interconnect two ormore adjacent staging capillaries 410. Each of the plurality ofmicrofluidic channels 406 can have a width and depth that is selected toachieve a desired capillary force. In some embodiments, the plurality ofmicrofluidic channels 406 can be arranged as a grouping 407 (FIG. 138).In some embodiments, assay input ports 402 can be positioned at apredetermined pitch (e.g. 9 mm) such that a central axis of each assayinput port 402 can be aligned with a center or other predeterminedportion of each grouping 407. Additionally, as discussed herein, atleast some of the plurality of microfluidic channels 406 can compriseramp features, surface treatments, and/or other features to achievedesired filling characteristics. These characteristics may varydepending on the size of staging capillaries 410, the type of assay1000, the necessary fill times, and the like. As illustrated in FIG.127, in some embodiments, the plurality of open slots 1922 formed ininput layer 404 can be sized such that, other than the coverage of assayinput ports 402, the plurality of microfluidic channels 406 and theplurality of staging capillaries 410 are exposed directly to atmospherewithout the need for venting shafts, tubes, conduits, or channels. Insome embodiments, the plurality of open slots 1922 can substantiallysurround assay input ports 402. Accordingly, the present of internalvacuums created during centrifuge can be reduced by either the pluralityof open slots 1922 or high aspect ratios of the plurality ofmicrofluidic channels 406, or a combination thereof.

During filling of embodiments employing the plurality of open slots 1922(see FIGS. 140-143), assay 1000 is first injected into assay input ports402 of input layer 404 (FIGS. 140-141). Capillary forces and/orgravitational pressures urge assay 1000 into the plurality ofmicrofluidic channels 406 and along the particular fluidic path (seeFIGS. 142-143). The stronger capillary force of the plurality of stagingcapillaries 410 draws assay 1000 therein from the plurality ofmicrofluidic channels 406. As illustrated in FIGS. 136-137, once theplurality of staging capillaries 410 have been filled with assay 1000,filling apparatus 400 and microplate 20 are centrifuged in a swing-armstyle centrifuge, which serves to overcome the surface tension and/orcapillary force of assay 1000 within the plurality of stagingcapillaries 410, to urge assay 1000 from the plurality of stagingcapillaries 410 to the plurality of wells 26 of microplate 20.

Assay Ports on Sides

In some embodiments, as illustrated in FIGS. 47-58, filling apparatus400 can comprise assay input ports 402 positioned within and/or uponoutput layer 408. In some embodiments, as illustrated in FIG. 47, assayinput ports 402 can be positioned at an end 420 of output layer 408. Forexample, such assay input ports can be positioned along a shortdimension of a major surface (e.g., a top surface) of the output layer,adjacent and parallel to an end thereof. In some embodiments, asillustrated in FIG. 48, assay input ports 402 can be positioned at aside 422 of output layer 408. For example, such assay input ports can bepositioned along a long dimension of a major surface (e.g., a topsurface) of the output layer, adjacent and parallel to a side thereof.Still further, in some embodiments, as illustrated in FIG. 49, assayinput ports 402 can be positioned at opposing ends 420 or opposing sides422 (not illustrated) of output layer 408. In some embodiments, assayinput ports 402 can be positioned at opposing ends 420 or opposing sides422 (not illustrated) of output layer 408 with a fluid interrupt 409(e.g. wall or barrier) to fluidly isolate those assay input ports 402 onone end or side from the remaining assay input ports 402 on the otherend or side.

As illustrated in FIG. 50, in some embodiments, assay input ports 402can each comprise a fluid well 424 bound by a plurality of upstandingwalls 426. In some embodiments, fluid well 424 of each assay input port402 can be in fluid communication with one or more correspondingmicrofluidic channels 406 through a throat 430 formed in fluid well 424.For example, such a throat can be formed in a lower region of the fluidwell, so as to fluidly communicate the fluid well with the microfluidicchannels. Throat 430 can comprise a diameter of, for example, 2 mm orless, 1 mm or less, 0.5 mm or less, or 0.25 mm or less. In someembodiments, such as illustrated in FIG. 50, throat 430 comprises areservoir in fluid communication with one or more microfluidic channel406. In some embodiments, surface tension relief post 418 can bedisposed in throat 430 to, at least in part, evenly spread assay 1000throughout the plurality of microfluidic channels 406 and/or engage ameniscus of assay 1000 to encourage fluid flow. Surface tension reliefpost can, according to some embodiments, comprise a hydrophilic sites inorder to further encourage fluid flow into the throat and, thus, themicrochannels.

In some embodiments, as illustrated in at least FIGS. 51-58,microfluidic channels 406 can be in fluid communication with theplurality of staging capillaries 410 extending from microfluidic channel406, through output layer 408, to a bottom surface 429. In someembodiments, bottom surface 429 can be spaced apart from first surface22 of microplate 20 (FIG. 51) or can be in contact with first surface 22of microplate 20. In some embodiments, each of the plurality of stagingcapillaries 410 can be generally aligned with a corresponding one of theplurality of wells 26 of microplate 20. In some embodiments, aprotective covering (not shown) can be disposed over microfluidicchannels 406 to provide, at least in part, protection fromcontamination, reduced evaporation, and the like. It should beunderstood that such protective covering can be used with any of thevarious configurations set forth herein.

Referring to FIGS. 52-58, to perform a filling operation, each assayinput port 402 can be at least partially filled with assay 1000 ordifferent assays or fluids (FIG. 52). At least in part through hydraulicpressure and/or capillary force, assay 1000 can flow from fluid well 424of each assay input port 402 through throat 430 into the one or moremicrofluidic channels 406 (FIG. 53). As assay 1000 flows across anend-opening or mouth 432 of each of the plurality of staging capillaries410, capillary action, at least in part, draws a metered amount of assay1000 therein (FIG. 54). Assay 1000 can continue to flow down the one ormore microfluidic channels 406 until each of the plurality of stagingcapillaries 410 can be at least partially filled with assay 1000 (FIG.55). In some embodiments, assay 1000 in each of the plurality of stagingcapillaries 410 can be held therein by capillary or surface tensionforces to aid in the equal metering of assay 1000 to be loaded in eachof the plurality of wells 26. In some embodiments, outlet 434 of each ofthe plurality of staging capillaries 410 permits venting of air withineach of the plurality of staging capillaries 410 during filling.

As illustrated in FIGS. 56 and 57, in some embodiments, fillingapparatus 400 can be stake cut, generally indicated at 435, via device436 along a portion of one or more microfluidic channels 406. In someembodiments, stake-cutting serves to, at least in part, aid in meteringof assay 1000 in each well 26 by isolating the plurality of stagingcapillaries 410 from any excess assay 1000 left in each assay input port402. This arrangement can minimize additional assay 1000 left withineach assay input port 402 from overfilling each of the plurality ofwells 26 during later centrifugation. In some embodiments, stake cuttingcan be completed through mechanical and/or thermal deformation (e.g.heat staking) of output layer 408. It should be appreciated that a Zbigvalve can be used to achieve fluid isolation between the plurality ofstaging capillaries 410 and assay input port 402, such as thosedescribed in commonly-assigned U.S. patent application Ser. No.10/336,274, filed Jan. 3, 2003 and PCT Application No. WO 2004/011147A1.

As illustrated in FIG. 59, in some embodiments, filling apparatus 400can comprise reduced material areas 438 disposed in output layer 408. Insome embodiments, reduced-material areas 438 comprise one or more cutoutportions 440 (e.g. voids, slots, holes, grooves) formed in output layer408 on opposing sides of microfluidic channels 406. The use of reducedmaterial areas 438 can provide, among other things, reduced thermalcapacity in the localized areas, which can increase the rate of heatstaking and/or stake cutting. In some embodiments, the elongated shapeof cutout portion 440 can accommodate any misalignment of the stakingtool relative to output layer 408. In some embodiments, followingstaking, excess assay 1000 in assay input ports 402 and/or the upstreamportion of microfluidic channels 406 relative to stake cut 435 can beremoved, if desired. In some embodiments, this can be accomplished byemploying a wicking member 441, as illustrated in FIG. 58.

In some embodiments, once at least some of the plurality of stagingcapillaries 410 are filled, output layer 408 and microplate 20 can beplaced into a swing-arm centrifuge. In some embodiments, the centripetalforce of the swing-arm centrifuge can be sufficient to overcome thesurface tension of assay 1000 in each the plurality of stagingcapillaries 410, thereby forcing a metered volume of assay 1000 intoeach of the plurality of wells 26 of microplate 20 (FIG. 60).

Referring again to FIGS. 47-49, filling apparatus 400 can be configuredin any one of a number of configurations as desired. As described above,as illustrated in FIG. 47, assay input ports 402 can be positioned atend 420 of output layer 408. When this configuration is used with amicroplate comprising 6,144 wells, filling apparatus 400 can comprise,for example, eight assay input ports 402 that can each be in fluidcommunication with eight respective microfluidic channels 406. Each ofthe eight microfluidic channels 406 can be in fluid communication withninety-six respective staging capillaries 410. In some embodiments, asillustrated in FIG. 48, assay input ports 402 can be positioned at side422 of output layer 408. When this configuration is used with amicroplate comprising 6,144 wells, filling apparatus 400 can comprise,for example, eight assay input ports 402 that can each be in fluidcommunication with twelve respective microfluidic channels 406. Each ofthe twelve microfluidic channels 406 can be in fluid communication withsixty-four respective staging capillaries 410. This configuration canprovide shorter channel lengths, which, in some circumstances, can havemore rapid capillary filling times relative to the configuration of FIG.47.

In some embodiments, as illustrated in FIG. 49, assay input ports 402can be positioned at opposing ends 420 or opposing sides 422(configuration not illustrated) of output layer 408. When theconfiguration illustrated in FIG. 49 is used with a microplatecomprising 6,144 wells, filling apparatus 400 can comprise, for example,sixteen assay input ports 402 that can each be in fluid communicationwith twelve respective microfluidic channels 406. Each of the twelvemicrofluidic channels 406 can be in fluid communication with thirty-tworespective staging capillaries 410. Likewise, when sixteen assay inputports 402 are positioned along opposing sides 422, sixteen assay inputports 402 can each be in fluid communication with eight respectivemicrofluidic channels 406. Each of the eight microfluidic channels 406can be in fluid communication with forty-eight respective stagingcapillaries 410. These configurations can provide shorter channellengths, which, in some circumstances, can have more rapid capillaryfilling times relative to the configurations of FIGS. 47 and 48.

In some embodiments, the plurality of microfluidic channels 406 can beoriented such that, during centrifugation, they are perpendicular to anaxis of revolution of the centrifuge. In some embodiments, thisorientation can limit the flow of assay 1000 along the plurality ofmicrofluidic channels 406 during centrifugation.

Overfill Solutions

In some embodiments, metering a predetermined amount of assay 1000 intoeach of the plurality of staging capillaries 410 and finally into eachof the plurality of wells 26 can be achieved using a plurality ofoverfill reservoirs disposed in output layer 408. Referring to FIGS.61-66, in some embodiments, filling apparatus 400 comprises fluid well424 in fluid communication with one or more corresponding microfluidicchannels 406 in fluid communication with the plurality of stagingcapillaries 410. In some embodiments, at least one microfluidic channel406 comprises one or more fluid overfill reservoir 442 in fluidcommunication therewith. In some embodiments, the one or more fluidoverfill reservoir 442 can be a bore opened at one end (e.g., a boreextending into output layer 408 from a surface thereof; with the borehaving an open upper-end and a closed bottom end.)

As illustrated in FIGS. 61-66, to perform a filling operation, eachassay input port 402 can be at least partially filled with assay 1000 orother desired fluid (FIG. 61). At least in part through hydraulicpressure and/or capillary force, assay 1000 can flow from fluid well 424of each assay input port 402 into the one or more microfluidic channels406 (FIG. 61). As assay 1000 flows across an upper-end opening or mouth432 of each of the plurality of staging capillaries 410, capillaryaction, at least in part, draws a metered amount of assay 1000 therein(FIG. 62). Assay 1000 can continue to flow down the one or moremicrofluidic channels 406 until each of the plurality of stagingcapillaries 410 can be at least partially filled with assay 1000 (FIG.63). In some embodiments, fluid overfill reservoir 442 can generallyinhibit assay 1000 from flowing into fluid overfill reservoir 442, atleast in part because of the single opening therein generally preventingair within fluid overfill reservoir 442 from exiting. In someembodiments, fluid overfill reservoir can have a diameter equal to thatof staging capillaries 410 and a depth of about 0.05 inch, or less.

In some embodiments, assay 1000 in each of the plurality of stagingcapillaries 410 can be held therein by capillary or surface tensionforces to aid in the equal metering of assay 1000 to be loaded in eachof the plurality of wells 26. In some embodiments, a lower-end openingor open-air outlet 434 of each of the plurality of staging capillaries410 permit venting of air within each of the plurality of stagingcapillaries 410 during filling.

As illustrated in FIGS. 64 and 65 and described above, in someembodiments, filling apparatus 400 can be stake cut, generally indicatedat 435, via device 436 along a portion of one or more microfluidicchannels 406. It should be appreciated that stake-cutting or staking canbe carried out, as previously described.

In some embodiments, once at least some of the plurality of stagingcapillaries 410 are filled, at least output layer 408 and microplate 20can be placed into a swing-arm centrifuge. In some embodiments, thecentripetal force of the centrifuge can be sufficient to overcome thecapillary force and/or surface tension of assay 1000 in each theplurality of staging capillaries 410, thereby forcing a metered volumeof assay 1000 into each of the plurality of wells 26 of microplate 20(FIG. 66). In some embodiments, the centripetal force of the centrifugecan be sufficient to force overfill fluid (e.g. assay 1000 stillremaining in microfluidic channels 406) into overfill reservoir 442,thereby displacing the air within overfill reservoir 442, rather thaninto the plurality of staging capillaries 410. In some embodiments, thisair can serve to isolate one staging capillary 410 from an adjacentstaging capillary 410. In some embodiments, overfill reservoir 442 canact as a reservoir for excess assay 1000. As illustrated in FIG. 67, insome embodiments, overfill reservoir 442 can be disposed within outputlayer 408 and generally aligned with and positioned below at least oneassay input port 402 in output layer 408.

Microfluidic Channel Shapes

As illustrated in FIGS. 68( a)-(g) and 69(a)-(g), in some embodiments,microfluidic channels 406 can have any one or a combination of variousconfigurations. In some embodiments, as illustrated in FIG. 68( a), eachmicrofluidic channel 406 can be in fluid communication with a pair ofrows of the plurality of staging capillaries 410 via feeder channels444. In some embodiments, as illustrated in FIGS. 68( b), 69(a), and69(c), microfluidic channel 406 can be in fluid communication with a rowof staging capillaries 410 that can be offset to one side ofmicrofluidic channel 406. In some embodiments, as illustrated in FIGS.68( c)-(e) and 69(d)-(f), a cross dimension, e.g., width, ofmicrofluidic channel 406 can vary relative to a diameter of each of theplurality of staging capillaries 410 ranging from larger than thediameter of each staging capillaries 410 to about equal to the diameterof each staging capillaries 410 to less than the diameter of eachstaging capillary (FIGS. 25( e)-(f)). In some embodiments, asillustrated in FIGS. 68( f), 68(g), 69(a), and 69(b), microfluidicchannel 406 can have a generally triangular cross-section that can beeither aligned with or offset from staging capillaries 410. In someembodiments, as illustrated in FIG. 69( g), microfluidic channel 406 canhave a single channel portion 446 fluidly coupled to two or more rows ofstaging capillaries 410. In some embodiments, single channel portion 446comprises a centrally disposed feature 448 to, in part, aid in fluidsplitting between adjacent rows of staging capillaries 410.

In some embodiments, capillary or surface tension forces encourage flowof assay 1000 through microfluidic channels 406. In this regard,microfluidic channels 406 can be of capillary size, for example,microfluidic channels 406 can be formed with a width of less than about500 micron, and in some embodiments less than about 125 microns, lessthan about 100 microns, or less than about 50 microns. In someembodiments, microfluidic channels 406 can be formed, for example, witha depth of less than about 500 micron, and in some embodiments less thanabout 125 microns, less than about 100 microns, or less than about 20microns. To further encourage the desired capillary action inmicrofluidic channels 406, microfluidic channels 406 can be providedwith an interior surface that is hydrophilic, i.e., wettable. Forexample, the interior surface of microfluidic channels 406 can be formedof a hydrophilic material and/or treated to exhibit hydrophiliccharacteristics. In some embodiments, the interior surface comprisesnative, bound, or covalently attached charged groups. For example, onesuitable surface, according to some embodiments, is a glass surfacehaving an absorbed layer of a polycationic polymer, such aspoly-l-lysine.

Capillary Overflow Control

In some embodiments, filling apparatus 400 can comprise an overflowretention system 1950 to receive and/or contain overflow of assay 1000during filling of the plurality of staging capillaries 410. In someembodiments, overflow retention system 1950 can improve the fillingaccuracy of each of the plurality of staging capillaries 410. In otherwords, prior art systems employing simply pipetting of sample into aplate can yield varying volumes of sample due to the infrequentcalibration of pipettes. Accordingly, in some embodiments, it can bebeneficial to include overflow retention system 1950 to at least in partimprove filling accuracy of assay 1000 in the plurality of stagingcapillaries 410, minimize waste of assay 1000, and enable use ofpipettes for initial loading.

In some embodiments, as illustrated in FIGS. 144-148, overflow retentionsystem 1950 can comprise one or more delay-filled capillaries 1952positioned downstream from one or more staging capillaries 410. In thisregard, the plurality of staging capillaries 410 upstream fromdelay-filled capillary 1952 are first filled with assay 1000 via theplurality of microfluidic channels 406. That is, staging capillary 410 awill first fill, then staging capillary 410 b to staging capillary 410n, until finally excess assay 1000 can be taken up by delay-filledcapillary 1952 through capillary action. During centrifugation, assay1000 disposed in delay-filled capillaries 1952 remains separate fromthat in or above the plurality of staging capillaries 410, therebypreventing or at least minimizing overfilling of well 26 of microplate20. In some embodiments, delay-filled capillaries 1952 can be smallerthan the plurality of staging capillaries 410 to create a relativelyhigher capillary force on assay 1000. In doing so, the higher capillaryforce in delay-filled capillaries 1952 can ensure that assay 1000remains therein during centrifugation.

During filling of embodiments employing delay-filled capillaries 1952(see FIGS. 145-148), assay 1000 is first injected into assay input ports402 of input layer 404 (FIG. 145). Capillary forces and/or gravitationalpressures urge assay 1000 into the plurality of microfluidic channels406 and along the particular fluidic path (see FIGS. 146-147). Thestronger capillary force of the plurality of staging capillaries 410 candraw assay 1000 therein from the plurality of microfluidic channels 406.Finally, excess assay 1000 reaches delay-filled capillaries 1952 and isdrawn therein through capillary action. As illustrated in FIG. 148, oncethe plurality of staging capillaries 410 have been filled with assay1000 and the excess drawn in to delay-filled capillaries 1952, fillingapparatus 400 and microplate 20 are centrifuged in a swing-arm stylecentrifuge, which serves to overcome the surface tension and/orcapillary force of assay 1000 within the plurality of stagingcapillaries 410, to urge assay 1000 from the plurality of stagingcapillaries 410 to the plurality of wells 26 of microplate 20. Theexcess assay 1000 remains in delay-filled capillaries 1952 (FIG. 148).

In some embodiments, as illustrated in FIG. 149, overflow retentionsystem 1950 can comprise one or more delay-filled channels 1953positioned throughout the network of staging capillaries 410, inaddition to or in place of delay-filled capillaries 1952 positioned atthe end of a series of staging capillaries 410. In other words, asillustrated in FIG. 149, delay-filled channels 1953 can be positioned atstrategic points or randomly throughout output layer 408. In someembodiments, delay-filled channels 1953 can be open channels, separatefrom said plurality of microfluidic channels 406 and/or capillary plane1912, extending between adjacent staging capillaries 410 or microfluidicchannels 406 (FIG. 149). To delay filling thereof until after theplurality of staging capillaries 410 are filled, delay-filled channels1953 can be sized to have a capillary force less than the plurality ofstaging capillaries 410 and greater than capillary plane 1912. In thisregard, the plurality of staging capillaries 410 fill beforedelay-filled capillary 1952 are first filled with assay 1000 due totheir great capillary force. Delay-filled channels 1953 then fill withthe remaining assay 1000 from capillary plane 1912. Duringcentrifugation, assay 1000 disposed in delay-filled channels 1953 remainfluidly separate from that in or above the plurality of stagingcapillaries 410, thereby preventing or at least minimizing overfillingof well 26 of microplate 20.

In some embodiments, as illustrated in FIGS. 150-152, overflow retentionsystem 1950 can comprise an overflow moat 1954 to receive excess assay1000 therein during centrifugation. In some embodiments, overflow moat1954 can be a depression or countersunk feature having a bottom 1956 andside retaining walls 1958 in fluid communication with capillary plane1912. Overflow moat 1954 can be positioned below and generally alignedwith assay input port 402. During centrifugation, excess assay 1000 isurged and retained within overflow moat 1954 to prevent overflow ofassay 1000 into the plurality of staging capillaries 410. It should beunderstood that overflow moat 1954 can be sized such that overflow moat1954 does not encourage flow from capillary plane 1912 during filling,however does encourage flow and retention of excess assay 1000 duringcentrifugation. This arrangement serves to, at least in part, urge assay1000 to the plurality of staging capillaries 410 during filling. Onceagain, after centrifugation, only excess assay 1000 will remain inoverflow moat 1954 while the volumes of the plurality of stagingcapillaries 410 are dispensed.

In some embodiments, as illustrated in FIGS. 153-160, overflow retentionsystem 1950 can comprise one or more burst pockets 1960 disposed ininput layer 404. More particularly, as illustrated in FIG. 153, in someembodiments input layer 404 can comprise burst pockets 1960 formed on anunderside thereof. Burst pockets 1960 can be in fluid communication withassay input port 402 such that during centrifugation (particularly earlycentrifugation), excess assay 1000 can be driven into burst pockets 1960and retained therein to prevent or at least minimize overflow of assay1000 into the plurality of staging capillaries 410 and later into wells26. As illustrated in FIGS. 154-160, burst pockets 1960 can have anyshape conducive to receiving assay 1000 during centrifugation. In someembodiments, one or a pair of burst pockets 1960 can be in fluidcommunication with assay input port 402 through a communication line1962 (FIGS. 157 and 160). Additionally, in some embodiments, additionalburst pockets 1960 can be used at each assay input port 402, such asthree (FIG. 156), four (FIG. 158), or more. Burst pockets 1960 can besized to contain a typical amount of overflow assay 1000 therein.Likewise, communication lines 1962 can be sized to prevent substantialflow of assay 1000 therethrough during filing of the plurality ofstaging capillaries 410 yet permit flow of assay 1000 therethroughduring centrifugation. Additionally, in some embodiments, burst pockets1960 can be disposed along a plane separate or otherwise offset (in adirection orthogonal to the plane of the plurality of stagingcapillaries 410) from the plurality of microfluidic channels 406 and/orcapillary plane 1912 to further prevent or inhibit inadvertent flow ofassay 1000 into burst pockets 1960 prior to centrifugation. In this way,excess assay 1000 can remain in assay input port 402 after filling ofthe plurality of staging capillaries 410 and will then be driven or urgeinto communication lines 1962 and burst pockets 1960 under forcesexerted during initial centrifugation (see FIGS. 158-160).

Floating Inserts

In some embodiments, as illustrated in FIGS. 70-84, filling apparatus400 comprises output layer 408, a floating insert 460, a cover 464, portmember 467, or any combination thereof for loading assay 1000 into atleast some of the plurality of wells 26 in microplate 20.

In some embodiments, output layer 408 comprises one or more recessedregions or depressions 454 formed in an upper surface 456 of outputlayer 408. Each depression 454 can be, in some embodiments, sized and/orshaped to receive floating insert 460 therein. In some embodimentscomprising two or more depressions 454, at least one wall 458 can beused to separate each depression 454 to define grouping 407 of stagingcapillaries 410 of any desired quantity and orientation.

In some embodiments, as illustrated in FIG. 71, floating insert 460 anddepression 454 can together define a capillary gap 468 between a bottomsurface 470 of floating insert 460 and a top surface 472 of depression454. In some embodiments, capillary gap 468 can result from surfacevariations in bottom surface 470 of floating insert 460 and/or topsurface 472 of depression 454 and/or spacing gaps formed therebetween.It should be appreciated that capillary gap 468 can be quite small;therefore, the drawings of the present application may exaggerate thisfeature for ease of printing and understanding. In some embodiments,capillary gap 468 exhibits a capillary force sufficient to draw assay1000 there along and to mouth 432 of each staging capillary 410. In someembodiments, bottom surface 470 of floating insert 460 and/or topsurface 472 of depression 454 can be treated and/or coated to enhancethe hydrophilic properties of capillary gap 468. In some embodiments,capillary gap 468 can be in fluid communication with an aperture 462extend through floating insert 460. Aperture 462 can be centrallylocated relative to floating insert 460 or can be located to one sideand/or corner thereof. In some embodiments, aperture 462 comprises anassay receiving well 463 (FIG. 72-84). In such embodiments, port member467 is optional.

As illustrated in FIG. 71, in some embodiments, to reduce capillaryforce between a sidewall 474 of floating insert 460 and wall 458 ofdepression 454, the thickness of floating insert 460 and the depth ofdepression 454 can be minimized to shorten the length of any resultingcapillary channel and, thus, reduce the overall capillary force in thisregion. In some embodiments, as illustrated in FIGS. 72-84, floatinginsert 460 comprises a flanged base portion 490 to reduce the potentialcapillary surface between sidewall 474 of floating insert 460 and wall458 of depression 454. In some embodiments, a hydrophic surface can beemployed between floating insert 460 and wall 458 of depression 454 toreduce capillary force therebetween. In some embodiments, this hydrophicsurface can result from native material characteristics, treatments,coatings, and the like.

In some embodiments, as illustrated in FIGS. 74-79, floating insert 460can be shaped to, at least in part, achieve any particular capillaryand/or flow characteristics. In some embodiments, as illustrated inFIGS. 74-76, floating insert 460 can comprise a plurality of flowfeatures 478 to, at least in part, extend the capillary surface tofacilitate capillary flow. In some embodiments, for example, each of theplurality of flow features 478 comprises a post member 480 (FIG. 74)extending orthogonally from bottom surface 470 of floating insert 460.In some embodiments, post member 480 comprises a radiused root portion482 to facilitate capillary flow, if desired. In some embodiments, postmember 480 can be offset within the corresponding staging capillary 410and can, if desired, contact a sidewall of staging capillary 410. Insome embodiments, each of the plurality of flow features 478 comprises atapered member 484 (FIGS. 75-79) extending from bottom surface 470 offloating insert 460. In some embodiments, each of the plurality ofstaging capillaries 410 comprises a corresponding mating entrancefeature 486 (FIGS. 75, 77, and 78) to closely conform to each flowfeature 478 to define a transition capillary gap 488. Tapered member 484can be conically shaped (FIGS. 75-76) to closely conform to thecomplementarily-shaped mating entrance feature 486 in staging capillary410. It should be appreciated that in some embodiments, the plurality offlow features 478 can further serve to individually plug or seal eachcorresponding capillary 410 during centrifugation (FIG. 79).

In some embodiments, floating insert 460 can comprise any materialconducive to encourage capillary action along capillary gap 468, such asbut not limited to plastic, glass, elastomer, and the like. In someembodiments, floating insert 460 can be made of at least two materials,such that an upper portion can be made of a first material and a lowerportion can be made of a second material. In some embodiments, thesecond material can provide a desired compliancy, hydrophilicity, or anyother desire property for improved fluid flow and/or sealing of stagingcapillaries 410. In some embodiments, the tapered members can include aseal-facilitating film, coating, or gasket thereon.

In some embodiments, as seen in FIG. 71, cover 464 can be used, at leastin part, to retain floating insert 460 within each depression 454, ifdesired. In some embodiments, cover 464 comprises an aperture 466generally aligned with an aperture 462 of floating insert 460. In someembodiments, cover 464 comprises a pressure sensitive adhesive to, atleast in part, retain floating insert 460 within depression 454.

As illustrated in FIGS. 70 and 71, in some embodiments, port member 467comprises assay input port 402. In some embodiments, port member 467 cancomprise a material comprising sufficient weight such that duringcentrifugation, the centripetal force of port member 467 exerted uponfloating insert 460 and output layer 408 can aid in closing offcross-communication of fluid between adjacent staging capillaries 410,as the upper-end openings of staging capillaries 410 can be covered andsealed by the lower surface of floating insert 460. In some embodiments,port member 467 can be sized such that its footprint (e.g. the surfacearea of a bottom surface 476 of port member 467) can be smaller than theopening of depression 454 to aid in the exertion of centripetal force onfloating insert 460 during centrifuge.

In some embodiments, as illustrated in FIG. 80-82, to load each of theplurality of staging capillaries 410, a predetermined amount of assay1000 can be placed at each assay input port 402 when used with portmember 467 or receiving well 463. Capillary gap 468 can be sized toprovide sufficient capillary force to draw at least a portion of assay1000 from assay input port 402 or receiving well 463 into capillary gap468. The capillary force of capillary gap 468 can be, at least in part,due to the non-rigid connection between floating insert 460 and outputlayer 408. As illustrated in FIG. 81, as assay 1000 is drawn into andspreads about capillary gap 468, each of the plurality of stagingcapillaries 410 in fluid communication with capillary gap 468 can beginto fill, at least in part, by capillary force as described herein.

In some embodiments, once at least some of the plurality of stagingcapillaries 410 are filled, at least output layer 408 and microplate 20can be placed into a centrifuge. For example, the pieces can be clampedor otherwise held together, and then placed in a bucket centrifuge as aunit. In some embodiments, the centripetal force of the centrifuge canbe sufficient to overcome the capillary force and/or surface tension ofassay 1000 in each the plurality of staging capillaries 410, therebyforcing a metered volume of assay 1000 into each of the plurality ofwells 26 of microplate 20. In some embodiments, the centripetal force ofthe centrifuge can also cause floating insert 460 to be forced and,thus, pressed against top surface 472 of depression 454. In someembodiments, where port member 467 is installed (FIGS. 70 and 71) or anyadditional weight member 492 (FIGS. 83 and 84), this additional weightcan further apply a force upon floating insert 460 to force floatinginsert 460 against top surface 472 of depression 454. This force onfloating insert 460 against top surface 472 of depression 454 can helpto fluidly isolate each staging capillaries 410 from adjacent stagingcapillaries 410 for improved metering.

It should be appreciated that any component of filling apparatus 400,such as input layer 404, output layer 408, floating insert 460, cover464, port member 467, intermediate layer 494, vent layer 523, etc., cancomprise a plate, tile, disk, chip, block, wafer, laminate, and anycombinations thereof, and the like.

Sweep Loader

In some embodiments, as illustrated in FIGS. 161-168, filing apparatus400 can comprise a sweep loader 1974 that can sweep across microplate 20to fill the plurality of wells 26 contained therein with assay 1000.That is, as illustrated in FIGS. 161-163 and 169, microplate 20 cancomprise a substantially planar construction having first surface 22 andopposing second surface 24 (see FIGS. 12-19, 171, and 169). Firstsurface 22 comprises the plurality of wells 26 disposed therein orthereon. Each of the plurality of wells 26 is sized to receive assay1000. In some embodiments, microplate 20 can be partitioned intodiscrete and/or distinct well groupings 1976. Each of the distinct wellgroupings 1976 can be serviced by a separate and distinct sweep loader1974 such that each distinct well grouping 1976 can contain a whollydifferent assay 1000 and/or other materials that can be processedsimultaneously without concern for cross-contamination and the like.Additionally, such distinct well groupings 1976 can enable a number ofsmaller samples to be tested in a reduced number of runs to permiteconomies of scale and, thus, reduced costs. In some embodiments, suchas that illustrated in FIG. 161, microplate 20 can be divided into fourwell groupings 1976, wherein each well grouping 1976 contains ninety-sixwells 26. Each of wells 26 can be spaced about 1.25 mm apartcenter-to-center. Each well 26 can contain about 300 nanoliters of assay1000. However, it should be understood that other sizes and spacing ofwells 26 are possible. In some embodiments, microplate 20 can be moldedout of plastic or die cast out of aluminum or other metal. In fact, insome embodiments, microplate 20 can be metal or heat resistant plasticsince no plastic seal needs to be welded thereto.

In some embodiments, each of the plurality of wells 26 of microplate 20can be shaped as long and shallow volumes, as illustrated in FIG. 163.To achieve such shape, one can sweep a narrow ellipse in a circle sothat the axis of the sweep is above surface 22 of microplate 20. Thelong axis of each well 26 can be tilted slightly so that the pluralityof wells 26 can be closely packed with the spacing roughly equal in eachdirection. This shape of wells 26 can be used in conjunction with sweeploader 1974 such that as sweep loader 1974 sweeps over the surface ofwell grouping 1976, assay 1000 is introduced into each well 26 andexcess assay 1000 is wiped away in a single pass. This shape of wells 26further minimize air bubbles from being trapped as assay 1000 enters theplurality of wells 26. As will be discussed herein, sweep loader 1974can further deposit a layer of oil or similar sealing material overmicroplate 20 following loadings. To further facilitate filling, each ofthe plurality of wells 26 can be hydrophilic, either through inherentmaterial properties, through coatings, and the like. Likewise, in someembodiments, the top surface of microplate 20 can be hydrophobic, eitherthrough inherent material properties, through coatings, and the like, todirect assay 1000 toward each of the plurality of wells 26 or otherwisedirect assay 1000 to a predetermine location or direction.

Still referring to FIGS. 161-163, 167, and 169, microplate 20 cancomprise a track system 1978 for receiving and/or guiding sweep loader1974. Track system 1978 can comprise upright walls 1980 disposed onopposing sides of well grouping 1976 that engage correspondingly sizedflange members extending downward from sweep loader 1974, as will bedescribed herein. Accordingly, in some embodiments, a top surface ofwell grouping 1976 can be lower than a periphery of microplate 20 tofurther define such separate and distinct well groupings 1976. In someembodiments, microplate 20 can comprise one or more assay overflowreservoirs 1982 disposed at an end(s) of well grouping 1976 to receiveexcess assay 1000 during filling of wells 26. Still further, in someembodiments, microplate 20 can comprise an area for staging sweeploaders 1974 in a position apart from the plurality of wells 26. Tosupport sweep loaders 1974 in this staging position (see FIG. 161),microplate 20 can comprise a pair of support arms 1984 for each sweeploader 1974. The pair of support arms 1984 can extend in a U-shape frommicroplate 20, such that track system 1978 extends to an end thereof toprovide seamless sliding movement of sweep loader 1974 from the stagingposition to a position over the plurality of wells 26 and then returnedto the staging position without interruption (see FIGS. 161 and 162). Toprevent overrun and/or to retain sweep loaders 1974 in the stagingposition, in some embodiments staging clips 1986 (FIG. 161) can be used.Staging clips 1986 can be generally W-shaped in profile such that afirst leg 1988 and center leg 1990 can capture and retain an end 1992 ofsupport arm 1984 of microplate 20. Furthermore, a second leg 1994 andcenter leg 1990 can capture and retain an upturned retaining feature1996 formed on sweep loader 1974. In some embodiments, second leg 1994can comprise a downwardly-turned feature 1998 sized to cooperate withupturned retaining feature 1996 of sweep loader 1974. It should beunderstood that any retaining mechanism could be use, although somebenefits of the present system may not be realized. Still further, insome embodiments, microplate 20 can comprise a physical stop member 2000to aid in capturing sweep loader 1974 in the staging position. It shouldalso be understood that microplates 20 having more than four wellgroupings 1976 can be used, such as for example a microplate 20 havingfourteen well groupings 1976 as illustrated in FIG. 169.

As illustrated in FIGS. 164-168, in some embodiments, sweep loader 1974comprises several features that aid in the deposition and filling of theplurality of wells 26 of microplate 20 with assay 1000. To this end,sweep loader 1974 can comprise an assay chamber 2002 adapted forreceiving assay 1000 therein having an input opening 2004 and an outputslot 2006. In some embodiments, output slot 2006 is sized to retainassay 1000 within assay chamber 2002 until such time that output slot2006 is spaced sufficiently close enough to the top surface of wellgrouping 1976 to create a capillary force to draw assay 1000 therefrom.In some embodiments, assay chamber 2002 can further comprise a neckedarea 2008 to maintain proper fluid pressures therein. In someembodiments, sweep loader 1974 comprises an oil chamber 2010. Oilchamber 2010 can be prefilled prior to distribution to an end user, ifdesired. In some embodiments, oil chamber 2010 is prefilled and a foillayer is disposed over an output slot 2012 of oil chamber 2010. In someembodiments, output slot 2012 of oil chamber 2010 can comprise a slopedsection 2014 to aid in directing oil over the plurality of wells 26during filling. In order to ensure the proper thickness of oil depositedover the plurality of wells 26, an oil scraper 2016 can be used. In someembodiments, oil scraper 2016 is positioned along an underside of sweeploader 1974 and is spaced a predetermined distance from the surface ofwell grouping 1976.

During filling, assay 1000 is loaded into assay chamber 2002 using anyknown technique and/or apparatus, such as a pipette. Sweep loader 1974can be them moved, either manually or via mechanical or robotic means,from the staging position to a position over the plurality of wells 26of microplate 20 at a controlled rate such that flanges 2022 extendingfrom a bottom thereof engage and guide sweep loader 1974 along tracksystem 1978. During this initial movement from the staging position, thefoil layer can be removed or otherwise ripped to reveal the oilcontained in oil chamber 2010. Once sweep loader 1974 is positioned overwell grouping 1976, a gap is formed between output slot 2006 of assaychamber 2002 and the upper surface of well grouping 1976 creating acapillary force urging a fluid bead of assay 1000 out of assay chamber2002, onto well grouping 1976, and finally into each of the plurality ofwells 26 under increases capillary force. Continued movement of sweeploader 1974 draws this fluid bead across well grouping 1976 filling allof the plurality of wells 26, while an assay scraper 2018 (FIG. 168) canbe employed behind this fluid bead to control deposition of assay 1000in some embodiments. Similarly during this time, a gap is formed betweenoutput slot 2012 of oil chamber 2010 and the upper surface of wellgrouping 1976 creating a capillary force urging an oil bead out of oilchamber 2010 and onto well grouping 1976 in the form of a protective oilseal over the plurality of wells 26. The thickness of this protectiveoil seal can be controlled by the specific dimensions of oil scraper2016. As sweep loader 1974 approaches the opposing end of well grouping1976, excess assay 1000 and/or oil can be received and containedoverflow reservoir 1982.

In some embodiments, once sweep loader 1974 contacts the opposing sideof microplate 20, wedge elevators 2020 raise sweep loader 1974 to breakthe assay fluid bead and the oil fluid bead to resist further flowthereof. More particularly, as illustrated in FIGS. 164-167, in someembodiments sweep loader 1974 comprise one or more wedge elevators 2020disposed adjacent to flanges 2020. Wedge elevators 2020 can be generallywedge shaped having a contact end 2024. Contact end 2024 is sized andpositioned to contact a fence 2026 formed at a far end of microplate 20(FIG. 162). Wedge elevator 2020 can be retained via any known method,such as spring wires 2028 and the like. During operation, wedgeelevators 2020 can contact fence 2026 after sweeping across theplurality of wells 26 causing wedge elevators 2020 to move from alowered position (FIG. 165) to a raised position (FIGS. 166 and 167).More particularly, a cam point 2030 of wedge elevator 2020 moves from afirst notch 2032 formed in the sidewall of sweep loader 1974 to a secondnotch 2034 formed in the sidewall. First notch 2032 can be higher on thesidewall of sweep loader 1974 relative to second notch 2034 causingsweep loader 1974 to be spaced closer to the plurality of wells 26. Alower rail edge 2036 of wedge elevators 2020 contacts a top surface 2038of track system 1978 to support sweep loader 1974 upon track system 1978during sliding movement. Once raised by virtue of contact between wedgeelevators 2020 and fence 2026, sweep loader 1974 can be slid back to thestaging position and snapped into place via staging clips 1986.

Surface Wipe

As illustrated, for example, in FIGS. 85-92, in some embodiments,filling apparatus 400 does not include the plurality of microfluidicchannels 406. In some embodiments, for example, filling apparatus 400comprises output layer 408 and a surface wipe assembly 1800 for loadingassay 1000 into at least some of the plurality of wells 26 in microplate20. In some embodiments, surface wipe assembly 1800 comprises one ormore of a base support 1810, a drive assembly 1812, a funnel assembly1814, or any combination thereof.

In some embodiments, such as illustrated in FIG. 85, base support 1810can be a generally planar support member operable to support microplate20 and output layer 408 thereon. In some embodiments, base support 1810comprises an alignment feature 1818 that can engage correspondingalignment feature 58 (refer to previous figures) of microplate 20 and/oralignment feature 519 of output layer 408 to maintain microplate 20 andoutput layer 408 in a predetermined alignment relative to each otherand/or funnel assembly 1814.

In some embodiments, drive assembly 1812 comprises a drive motor 1816; aguide member 1820, coupled to or formed in base support 1810; a trackingmember 1822, coupled to or formed in funnel assembly 1814; and controlsystem 1010. In some embodiments, guide member 1820 and tracking member1822 are sized and/or shaped to slidingly engage with each other toprovide guiding support for funnel assembly 1814 as it moves relative tobase support 1810. In some embodiments, drive motor 1816 can be operablycoupled to tracking member 1822 or base support 1810 to move trackingmember 1822 relative to guide member 1820 via known drive transmissioninterfaces, such as mechanical drives, pneumatic drives, hydraulicdrives, electromechanical drives, and the like. In some embodiments,drive motor 1816 can be controlled in response to control signals fromcontrol system 1010 or a separate control system. In some embodiments,drive motor 1816 can be operably controlled in response to a switchdevice controlled by a user.

In some embodiments, funnel assembly 1814 comprises a spanning portion1824 generally extending above output layer 408. In some embodiments,spanning portion 1824 can be supported on opposing ends by trackingmember 1822 of drive assembly 1812 and a foot member 1826. Trackingmember 1822 and foot member 1826 can each be coupled to spanning portion1824 via conventional fasteners in some embodiments. Foot member 1826can be generally arcuately shaped so as to reduce the contact areabetween foot member 1826 and base support 1810. In some embodiments,foot member 1826 can be made of a reduced friction material, such asDelrin®.

In some embodiments, spanning portion 1824 of funnel assembly 1814comprises a slot 1828 formed vertically therethrough that can be sizedand/or shaped to receive a funnel member 1830 therein. As illustrated inFIGS. 85-92, funnel member 1830 can comprise one or more assay chambers1832 for receiving one or more different assays therein. It should beappreciated that drive assembly 1812 and funnel assembly 1814 can beconfigured to track in a direction perpendicular to that illustrated inthe accompanying figures to provide an increased number of assaychambers 1832 and reduced track distances. In some embodiments, such asillustrated in FIG. 86, funnel member 1830 can comprise a flange portion1834 extending about a top portion thereof. Flange portion 1834 offunnel member 1830 can be sized and/or shaped to rest upon acorresponding flange portion 1836 of slot 1828 of spanning portion 1824to support funnel member 1830. However, it should be appreciated thatfunnel member 1830 can comprise any outer profile complementary to slot1828.

Assay chambers 1832, in some embodiments, can be shaped to provide apredetermined assay capacity for filling all of a predetermined numberand/or grouping of the plurality of staging capillaries 410 in outputlayer 408. In some embodiments, assay chamber 1832 comprises convergingsidewalls 1838 that terminate at a tip portion 1840.

In some embodiments, such as illustrated in FIG. 87-89, to load each ofthe plurality of staging capillaries 410, a predetermined amount ofassay 1000 can be placed in each assay chamber 1832. In someembodiments, each assay chamber 1832 comprises a different assay. Assay1000 is drawn down along sidewalls 1838 to tip portion 1840 to form afluid bead 1842 extending from tip portion 1840 that can be in contactwith upper surface 456 of output layer 408. In some embodiments, driveassembly 1812 can be actuated to advance funnel assembly 1814 acrossoutput layer 408 at a predetermined rate, as illustrated in FIG. 88.However, it should be appreciated that funnel assembly 1814 can beadvanced manually across output layer 408. As funnel assembly 1814 isadvanced across output layer 408, in some embodiments, fluid bead 1842can contact the upper-end opening or entrance of each of the pluralityof staging capillaries 410 and begin to fill, at least in part, bycapillary force as described herein.

As illustrated in at least FIGS. 86-89, 91, and 98, in some embodiments,fluid bead 1842 can be bound by a lip or wiper member 1844 extendingdownwardly from tip portion 1840 of funnel member 1830. In someembodiments, wiper member 1844 can, at least in part, wipe and/or removeexcess assay 1000 on upper surface 456 of output layer 408 as funnelmember 1830 moves thereabout. In some embodiments, a sponge or otherporous material member 1845 can be disposed, positioned, or otherwisefixed to tip portion 1840 of funnel member 1830 (FIG. 91). Porousmaterial member 1845 can, at least in part, serve to control and/ormeter assay 1000 into the plurality of staging capillaries 410. In otherwords, porous material member 1845 can serve as a physical barrier toinhibit free flow of assay 1000. The size and shape of the plurality ofair pockets within porous material member 1845 can be selected toinhibit such free flow of assay 1000. However, during dispensing and/orfilling, porous material member 1845 can be compressed or otherwisedeformed to displace the air within the plurality of air pockets topermit flow of assay 1000 therethrough. The degree of assay flowprevention or ease of liquid passage can be controlled by at least thefollowing parameters of porous material member 1845: pore size,durometer, and any surface treatments to vary the surface chemistries(i.e., make it more or less hydrophobic or hydrophilic).

In some embodiments, such as illustrated in FIGS. 85 and 89, as funnelassembly 1814 continues past the last of the plurality of stagingcapillaries 410, some assay 1000 can be forced off upper surface 456 ofoutput layer 408 at an edge 1846 into at least one overflow channel1848. In some embodiments, once at least some of the plurality ofstaging capillaries 410 are filled, at least output layer 408 andmicroplate 20 can be placed into a centrifuge. In some embodiments, thecentripetal force of the centrifuge can be sufficient to overcome thecapillary force and/or surface tension of assay 1000 in each theplurality of staging capillaries 410, thereby forcing a metered volumeof assay 1000 into each of the plurality of wells 26 of microplate 20.

In some embodiments, such as illustrated in FIG. 85, the excess assay1000 in overflow channel 1848 can be contained using one or morereservoir pockets 1850. In some embodiments, reservoir pocket 1850 canbe in fluid communication with at least one overflow channel 1848. Insome embodiments, reservoir pocket 1850 can be deeper than overflowchannel 1848 to encourage flow of assay 1000 to reservoir pocket 1850.During centrifugation, centripetal force can further encourage assay1000 to flow to reservoir pocket 1850, thereby reducing the likelihoodof any contamination or cross-feed between adjacent staging capillaries410. In some embodiments, an extended wall member 1852 can be positionedabout reservoir pocket 1850 to further contain assay 1000.

In some embodiments, such as illustrated in FIGS. 90 and 91, the excessassay 1000 in overflow channel 1848 can be contained using a reservoirtrough 1854. In some embodiments, an absorbent member 1856 can bedisposed in reservoir trough 1854 to absorb excess assay 1000 therein.In some embodiments, absorbent member 1856 can be a hydrophilic fibermembrane. As illustrated in FIG. 91, reservoir trough 1854 can be slopedtoward absorbent member 1856 to facilitate absorption of excess assay1000. In some embodiments, absorbent member 1856 can be removable topermit removal and relocating of the excess assay 1000 prior tocentrifugation.

In some embodiments, such as illustrated in FIGS. 92 and 93, funnelmember 1830 can comprise two or more discrete assay chambers 1832 fordelivering one or more different assays. In such embodiments, forexample, output layer 408 can comprise one or more central overflowchannels 1858 extending along upper surface 456 of output layer 408 toreceive at least some overflow assay 1000. In some embodiments, centraloverflow channels 1858 are each disposed between each separate groupingof staging capillaries 410 served by each discrete assay chamber 1832.In some embodiments, as illustrated in FIG. 92, central overflow channel1858 can be sloped down to at least one of overflow channel 1848 (FIG.85), reservoir pocket 1850 (FIG. 85), reservoir trough 1854 (FIG. 90),or absorbent member 1856 (FIG. 92). As illustrated in FIG. 93, in someembodiments, absorbent member 1856 can be sized and/or shaped to fitwith an enlarged reservoir pocket 1850.

In some embodiments, as illustrated in FIGS. 171-172, output layer 408can comprise one or more central hydrophobic lines or features 1970extending along upper surface 456 of output layer 408. In someembodiments, hydrophobic lines 1970 are each disposed between eachseparate grouping of staging capillaries 410 served by each discreteassay chamber 1832. In embodiments providing sufficient spacing betweenadjacent groupings and/or staging capillaries 410, hydrophobic lines1970 can be disposed between staging capillaries 410 (see FIG. 171).However, in embodiments providing less spacing between adjacentgroupings and/or staging capillaries 410, hydrophobic lines 1970 can bedisposed along a line of staging capillaries 410 (see FIG. 172) suchthat the upper opening of each staging capillary 410 along such line isopen to permit filling of assay 1000, but the space between stagingcapillaries 410 in that line is covered with such hydrophobic line 1970.The use of hydrophobic lines 1970 can provide reduced manufacturingcomplexity, compared to injection molding small walls or channels, andconsequently reduced manufacturing cost. Additionally, application ofhydrophobic lines 1970 can be completed in an operation separate frominitial manufacturing, thereby permitting economies of scale for outputlayers having differing shapes of staging capillary groups. In someembodiments, hydrophobic lines 1970 can be formed on output layer 408through pad printing, silk screening, plasma coating, and the like. Insome embodiments, hydrophobic lines 1970 can be made of PDMS, silicone,Teflon, paralene, any other hydrophobic material, or combinationsthereof.

Funnel Member

As illustrated in FIGS. 94-107, in some embodiments, funnel member 1830of funnel assembly 1814 can be any one of a number of configurationssufficient to maintain fluid bead 1842 in contact with upper surface 456of output layer 408. In some embodiments, a predetermined shape of fluidbead 1842 and/or a predetermined flowrate of assay 1000 through tipportion 1840 can be achieved through the particular configuration offunnel member 1830.

As illustrated in FIG. 94-96, in some embodiments, funnel member 1830comprises one or more assay chambers 1832 in fluid communication withtip portion 1840. As described above, in embodiments comprising two ormore assay chambers 1832 (FIG. 95), multiple assays can be used suchthat a different assay can be disposed in each assay chamber 1832. Itshould be understood that any number of assay chambers 1832 can be used(e.g., 2, 4, 6, 8, 10, 12, 16, 20, 32, 64, or more).

In some embodiments, tip portion 1840 can be configured to define acapillary force and/or surface tension sufficient to prevent assay 1000from exiting assay chamber 1832 prior to fluid bead 1842 engaging uppersurface 456 and to permit assay 1000 to be pulled into each of theplurality of staging capillaries 410 during filling of the stagingcapillaries. As illustrated in FIG. 97, tip portion 1840 comprises arestricted orifice 1860 that is sized to increase surface tension toretain assay 1000 with assay chamber 1832. In some embodiments, tipportion 1840 can be spaced apart from an underside surface 1862 to, atleast in part, inhibit assay 1000 from collecting between funnel member1830 and output layer 408. In some embodiments, as illustrated in FIG.98, restricted orifice 1860 can be used with wiper member 1844 toincrease surface tension to retain assay 1000 and to wipe and/or removeexcess assay 1000 on upper surface 456 of output layer 408. In someembodiments, such as illustrated in FIG. 99, tip portion 1840 cancomprise a planar cavity 1864 disposed in fluid communication withrestricted orifice 1860. In some embodiments, planar cavity 1864 canencourage the formation of wider and/or shallower fluid bead 1842relative to similar configurations not employing planar cavity 1864. Insome configurations, the wider and/or shallower fluid bead 1842 can, atleast in part, prolong the time fluid bead 1842 is in contact with eachof the plurality of staging capillaries 410.

As illustrated in FIG. 100, in some embodiments, funnel member 1830 cancomprise wiper 1844 spaced apart from tip portion 1840 to wipe and/orremove excess assay 1000 on upper surface 456 of output layer 408. Insome embodiments, wiper 1844 can extend a distance from undersidesurface 1862 of funnel member 1830 equal to about a distance fromunderside surface 1862 to a distal end of tip portion 1840. Asillustrated in FIGS. 101-103, each tip portion 1840 associated with eachassay chamber 1832 can be offset relative to adjacent tip portions 1840.In some embodiments, this offset relationship between adjacent tipportions 1840 can permit the plurality of staging capillaries 410 to beclosely spaced with reduced likelihood for crosstalk between adjacentfluid beads 1842.

Still referring to FIGS. 101-103, in some embodiments, restrictedorifice 1860 comprises an elongated slot 1866 (FIG. 101) generallyextending from one edge of tip portion 1840 to the opposing edge todefine an elongated fluid bead 1842. However, in some embodiments,restricted orifice 1860 comprises one or more apertures 1868. In someembodiments, the reduced cross-sectional area of apertures 1868 relativeto that of elongated slot 1866 can serve to withstand a fluid headpressure exerted by assay 1000 in assay chamber 1832 that wouldotherwise overcome the surface tension of fluid bead 1842 exitingelongated slot 1866 and possibly lead to premature discharge of assay1000. In some embodiments, the restricted orifice 1860 can be collinearas well as offset as illustrated in (FIG. 101).

In some embodiments, such as illustrated in FIGS. 104-106, funnel member1830 can comprise an internal siphon passage 1870 to, at least in part,control the flowrate of assay 1000 from restricted orifice 1860. In someembodiments, funnel member 1830 comprises a main chamber 1872 fluidlycoupled to a delivery chamber 1874 via siphon passage 1870. In someembodiments, siphon passage 1870 can be positioned along a bottom ofmain chamber 1872. Siphon passage 1870 can comprise an upturned section1876 that can require assay 1000 in main chamber 1872 to flow, at leastin part, against the force of gravity. In some embodiments, main chamber1872 and delivery chamber 1874 can be fluidly coupled at the top thereofby a top chamber 1878. When main chamber 1872 is filled at leastpartially above top chamber 1878, the excess assay 1000 can flow acrosstop chamber 1878 into delivery chamber 1874. During filling, as thelevel of assay 1000 drops below the bottom surface of top chamber 1878and assay 1000 flows from restricted orifice 1860, assay 1000 withindelivery chamber 1874 can be replaced through the siphoning action ofsiphon passage 1870 at the bottom of main chamber 1872. This arrangementcan reduce the fluid head pressure exerted at restricted orifice 1860.Accordingly, the fluid head pressure exerted at restricted orifice 1860can be generally to about the fluid head pressure of assay 1000contained in delivery chamber 1874.

In some embodiments, as illustrated in FIGS. 106 and 107, funnel member1830 can be formed with a two- or more-piece construction. Asillustrated in FIG. 106, funnel member 1830 can comprise a first section1880 and a second section 1882. First section 1880 can comprise one ormore desired features. For example, as illustrated in FIG. 106, upturnedsection 1876 of FIG. 105 can be formed in first section 1880. Firstsection 1880 and second section 1882 can then be joined or otherwisemated along a generally vertical joining line 1884 (FIG. 105) to formfunnel member 1830. In some embodiments, first section 1880 and secondsection 1882 can be joined or otherwise mated along a generallyhorizontal joining line 1886 (FIG. 107). In some embodiments, firstsection 1880 and second section 1882 can be made from differentmaterials to achieve a predetermined performance. In some embodiments,second section 1882 can be made of an elastomer to provide enhanceflexibility to accommodate for variations in output layer 408 andenhanced wiping performance of wiper member 1844.

Surface Treatment

In some embodiments, portions of filling apparatus 400 that are intendedto contact assay 1000, such as assay input ports 402, microfluidicchannels 406, the plurality of staging capillaries 410, and the like,can be hydrophilic. Likewise, in some embodiments, surfaces not intendedto contact assay 1000 can be hydrophobic.

In some embodiments, filling apparatus 400 comprises a treatment toincrease surface energy thereof to improve flow and/or capillary actionof any surface of filling apparatus 400 exposed to assay 1000, such asassay input ports 402, microfluidic channels 406, staging capillaries410, microfluidic channels 406, depression 454, upper surface 456, etc.In some embodiments, surface energy can be improved, for example, whenusing a polymer material in the manufacture of filling apparatus 400,through surface modification of the polymer material via Michaeladdition of acrylamide or PEO-acrylate onto laminated surface; surfacegrafting of acrylamide or PEO-acrylate via atom transfer radicalpolymerization (ARTP); surface grafting of acrylamide via Ce(IV)mediated free radical polymerization; surface initiated living radicalpolymerization on chloromethylated surface; coating of negativelycharged polyelectrolytes; plasma CVD of acrylic acid, acrylamide, andother hydrophilic monomers; or surface adsorption of an ionic ornon-ionic surfactant. In some embodiments, surfactants, such as thoseset forth in Tables 2 and 3, can be used.

TABLE 2 Surfactants for Coating Hydrophile Lipophile Balance No. Name MW(HLB) 1 Tetronic 901 4700 3 2 Tetronic 1107 1500 24 3 Tetronic 1301 68002 4 Poly(styrene-b-ethylene oxide) Mn: 3600–67000 5Poly(stryrene-b-sodium acrylate) Mn: 1800–42500 6 Triton X-100 13.5 7Triton X-100 reduced 8 Tween 20 1228 16.7 9 Tween 85 1839 11 10 Span 831109.56 3.7 11 Span 80 428.62 4.3 12 Span 40 402.58 6.7

TABLE 3 Surfactants for Wetting Polypropylene Acids: Dodecyl sulfate, Nasalt CH₂(CH₂)₁₁OSO₃ ⁻ Na⁺ Octadecyl sulfate, Na salt CH₃(CH₂)₁₇OSO₃ ⁻Na⁺ Quaternary ammonium compounds: Cetyltrimethylammonium bromideCH₃(CH₂)₁₅N⁺(CH₃)₃ Br⁻ Octadecyltrimethylammonium bromideCH₃(CH₂)₁₇N⁺(CH₃)₃Br⁻ Ethers: Brij-52 CH₃(CH₂)₁₅(OCH₂CH₂)₂OH Brij 56CH₃(CH₂)₁₅(OCH₂CH₂)₁₀OH Brij 58 CH₃(CH₂)₁₅(OCH₂CH₂)₂₀OH Brij 72CH₃(CH₂)₁₇(OCH₂CH₂)₂OH Brij 76 CH₃(CH₂)₁₇(OCH₂CH₂)₁₀OH Brij 78CH₃(CH₂)₁₇(OCH₂CH₂)₂₀OH Esters: Poly(ethylene glycol) monolaurateCH₃(CH₂)₁₀CO(OCH₂CH₂)_(4.5)OH Poly(ethyleneglycol) distearateCH₃(CH₂)₁₆—CO—(OCH₂)₉—O—CO—(CH₂)₁₆CH₃ Poly(ethyleneglycol)dioleateCH₃(CH₂)₇CH═CH(CH₂)₇—CO—(OCH₂)₉— O—CO—(CH₂)₇CH═CH(CH₂)₇CH₃

In some embodiments, filling apparatus 400 can comprise polyolefins;poly(cyclic olefins); polyethylene terephthalate;poly(alkyl(meth)acrylates); polystyrene; poly(dimethyl siloxane);polycarbonate; structural polymers, for example, poly(ether sulfone),poly(ether ketone), poly(ether ether ketone), and liquid crystallinepolymers; polyacetal; polyamides; polyimides; poly(phenylene sulfide);polysulfones; poly(vinyl chloride); poly(vinyl fluoride);poly(vinylidene fluoride); copolymers thereof; and mixtures thereof.

In some embodiments, a co-agent can be employed to enhance thehydrophilicity and/or improve the shelf life of filling apparatus 400.Co-agents can be, for example, a water-soluble or slightly water-solublehomopolymer or copolymers prepared by monomers comprising, for example,(meth)acrylamide; N-methyl(methyl)acrylamide,N,N-dimethyl(methyl)acrylamide, N-ethyl(meth)acrylamide,N-n-propyl(meth)acrylamide, N-iso-propyl(meth)acrylamide,N-ethyl-N-methyl(meth)acrylamide, N,N-diethyl(meth)acrylamide,N-hydroxymethyl(meth)acrylamide, N-(3-hydroxypropyl)(meth)acrylamide,N-vinylformamide, N-vinylacetamide, N-methyl-N-vinylacetamide, vinylacetate that can be hydrolyzed to give vinylalcohol afterpolymerization, 2-hydroxyethyl (meth)acrylate,3-hydroxypropyl(meth)acrylate, N-vinypyrrolidone, poly(ethylene oxide)(meth)acrylate, N-(meth)acryloxysuccinimide, N-(meth)acryloylmorpholine,N-2,2,2-trifluoroethyl (meth)acrylamide, N-acetyl(meth)acrylamide,N-amido(meth)acrylamide, N-acetamido (meth)acrylamide,N-tris(hydroxymethyl)methyl(meth)acrylamide,N-(methyl)acryloyltris(hydroxymethyl)methylamine, (methyl)acryloylurea,vinyloxazolidone, vinylmethyloxazolidone, and combinations thereof. Insome embodiments, the co-agent can be poly(acrylicacid-co-N,N-dimethylacrylamide) or poly(N,N-dimethylacrylamide-co-styrene sulfonic acid).

1. A filling system for receiving a sample comprising: an output layerhaving a plurality of capillaries, each of said plurality of capillarieshaving an inlet and an outlet, said output layer having at least onehydrophobic feature disposed thereon separating a first grouping of saidplurality of capillaries from a second grouping of said plurality ofcapillaries; and a surface wipe assembly comprising: a base supportingsaid output layer; and a funnel assembly engaging said base and moveablerelative to said base, said funnel assembly having a funnel member sizedto receive said sample, said funnel member having an outlet fordelivering a fluid bead of said sample along a top surface of saidoutput layer and in fluid communication with each of said plurality ofcapillaries such that a portion of said fluid bead is drawn within atleast some of the plurality of capillaries in response to capillaryforce, said funnel assembly and said output layer being moveablerelative to each other between a first position and a second position todraw said fluid bead across said top surface.
 2. The filling systemaccording to claim 1 wherein said at least one hydrophobic feature is aline extending substantially from one end of said output layer to anopposing end.
 3. The filling system according to claim 1 wherein saidhydrophobic feature is disposed between adjacent rows of said pluralityof capillaries.
 4. The filling system according to claim 1 wherein saidhydrophobic feature is disposed along a row of said plurality ofcapillaries.
 5. The filling system according to claim 1 wherein said atleast one hydrophobic feature is formed on said output layer through atleast one of pad printing, silk screening, and plasma coating.
 6. Thefilling system according to claim 1 wherein said at least onehydrophobic feature is made of at least one of PDMS, silicone, Teflon,and paralene.
 7. The filling system according to claim 1, furthercomprising: a drive assembly operably coupled to one of said outputlayer and said funnel assembly to provide said relative movement of saidfunnel assembly and said output layer between said first position andsaid second position.
 8. The filling system according to claim 7 whereinsaid drive assembly comprises: a drive motor operably coupled to one ofsaid output layer and said funnel assembly; and a control systemoperably coupled to said drive motor, said control system selectivelyactuating said drive motor in response to a control input.
 9. Thefilling system according to claim 8 wherein said drive assembly furthercomprises: said base support for supporting said output layer; a guidemember extending from said base support; and a tracking member extendingfrom said funnel assembly, said tracking member engagable with saidguide member to guide said funnel assembly relative to said outputlayer.
 10. The filling system according to claim 9 wherein said funnelassembly comprises: a spanning portion having a slot formedtherethrough; a funnel member disposed in said slot.
 11. The fillingsystem according to claim 1 wherein said output layer comprises: anoverflow channel formed therein, said overflow channel being in fluidcommunication with at least a portion of said top surface of said outputlayer.
 12. The filling system according to claim 1 wherein said funnelassembly comprises: a funnel member having a first sample chamber and asecond sample chamber, said first sample chamber being in fluidcommunication with said first grouping of said plurality of capillariesand said second sample chamber being in fluid communication with saidsecond grouping of said plurality of capillaries.
 13. The filling systemaccording to claim 1 wherein each of said plurality of capillaries issized to provide sufficient force to draw a predetermined volume of saidsample therein and permit release of said sample from each of saidplurality of capillaries in response to an applied centripetal force.14. A filling system for receiving a sample comprising: an output layerhaving a plurality of capillaries, each of said plurality of capillarieshaving an inlet and an outlet, said output layer having at least onehydrophobic feature separating a first grouping of said plurality ofcapillaries from a second grouping of said plurality of capillaries; anda surface wipe assembly comprising: a base supporting said output layer;and a funnel assembly engaging said base and moveable relative to saidbase, said funnel assembly having a first sample chamber and a secondsample chamber, said first sample chamber being in fluid communicationwith said first grouping of said plurality of capillaries and saidsecond sample chamber being in fluid communication with said secondgrouping of said plurality of capillaries, said first grouping beingseparate from said second grouping, said first sample chamber and saidsecond sample chamber delivering separate fluid beads of said samplealong said top surface of said output layer and in fluid communicationwith said first grouping and said second grouping respectively to drawat least a portion of said fluid bead in to at least some of theplurality of capillaries in response to capillary force.
 15. The fillingsystem according to claim 14 wherein said at least one hydrophobicfeature is a line extending substantially from one end of said outputlayer to an opposing end.
 16. The filling system according to claim 14wherein said hydrophobic feature is disposed between adjacent rows ofsaid plurality of capillaries.
 17. The filling system according to claim14 wherein said hydrophobic feature is disposed along a row of saidplurality of capillaries.
 18. The filling system according to claim 14wherein said at least one hydrophobic feature is formed on said outputlayer through at least one of pad printing, silk screening, and plasmacoating.
 19. The filling system according to claim 14 wherein said atleast one hydrophobic feature is made of at least one of PDMS, silicone,Teflon, and paralene.
 20. The filling system according to claim 14,further comprising: a drive assembly operably coupled to one of saidoutput layer and said funnel assembly to provide relative movement ofsaid funnel assembly and said output layer between a first position anda second position.
 21. The filling system according to claim 15 whereinsaid drive assembly comprises: a drive motor operably coupled to one ofsaid output layer and said funnel assembly; and a control systemoperably coupled to said drive motor, said control system selectivelyactuating said drive motor in response to a control input.
 22. Thefilling system according to claim 21 wherein said drive assembly furthercomprises: said base support for supporting said output layer; a guidemember extending from said base support; and a tracking member extendingfrom said funnel assembly, said tracking member engagable with saidguide member to guide said funnel assembly relative to said outputlayer.
 23. The filling system according to claim 22 wherein said funnelassembly comprises: a spanning portion having a slot formedtherethrough; a funnel member disposed in said slot.
 24. The fillingsystem according to claim 20 wherein said output layer comprises: anoverflow channel formed therein, said overflow channel being in fluidcommunication with at least a portion of said top surface of said outputlayer.
 25. The filling system according to claim 24 wherein said funnelassembly comprises: a funnel member having a first sample chamber and asecond sample chamber, said first sample chamber being in fluidcommunication with said first grouping of said plurality of capillariesand said second sample chamber being in fluid communication with saidsecond grouping of said plurality of capillaries.
 26. The filling systemaccording to claim 20 wherein each of said plurality of capillaries issized to provide sufficient force to draw a predetermined volume of saidsample therein and permit release of said sample from each of saidplurality of capillaries in response to an applied centripetal force.27. A method of distributing a sample comprising: providing the deviceof claim 1; and drawing a first fluid bead of a first sample across saidoutput layer such that at least a portion of said first fluid bead isdrawn within said first grouping of said plurality of capillaries. 28.The method according to claim 27 further comprising: drawing a secondfluid bead of a second sample across said output layer such that atleast a portion of said second fluid bead is drawn within a second ofsaid plurality of capillaries.